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Vitamin C to Decrease Effects of Smoking in Pregnancy on Infant Lung Function

Vitamin C to Decrease Effects of Smoking in Pregnancy on Infant Lung Function

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01723696
Acronym
VCSIP
Enrollment
252
Registered
2012-11-08
Start date
2012-12-31
Completion date
2017-12-31
Last updated
2019-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infant Wheeze, In-utero Nicotine, Pulmonary Function; Newborn, Abnormal, Second Hand Smoke

Keywords

In-utero smoke;, Pulmonary function testing;, Wheeze;, Vitamin C;, Forced expiratory flows

Brief summary

Vitamin C supplementation (500 mg per day) given to pregnant women who can not quit smoking will improve the pulmonary function tests in their offspring measured at 3 months of age.

Detailed description

Smoking during pregnancy remains a major public health problem as at least 12% of pregnant women cannot quit smoking during pregnancy. This addiction is the largest preventable cause of childhood respiratory illness, including asthma, and children whose mothers smoked during pregnancy show lifetime decreases in pulmonary function. Smoking is a unique morbidity in that it is addictive, heavily advertised and recent genome studies show there are genotypes that significantly increase the likelihood of being unable to quit. Teen pregnancy, low income, low education, and living with another smoker are important factors increasing the odds of smoking during pregnancy. Pulmonary function tests done shortly after birth in babies born to mothers who smoked during pregnancy show decreased pulmonary function as measured by decreased respiratory flows and respiratory compliance and altered tidal breathing patterns. These changes can still be measured even after the infants have reached adulthood. Multiple epidemiologic studies show that these decreases in pulmonary function lead to increased respiratory disease and costs of hundreds of millions of dollars per year. The primary aim of this double-blind, placebo controlled, randomized, multi-site study is to demonstrate improved pulmonary function testing at 3 months of age, in infants delivered to smoking mothers who are randomized to 500 mg/day of supplemental vitamin C versus placebo at less than or equal to 22 weeks of pregnancy. We will recruit 278 smoking pregnant women into the study. Patients will meet with research personnel at each prenatal visit and smoking cessation will be actively encouraged. Patients will be monitored with a set of serial biomarkers to assess smoking and medication compliance, including urine cotinine levels, smoking questionnaires, pill counts and fasting plasma ascorbic acid levels. Pulmonary function tests will be done at 3 months of age and will measure forced expiratory flows. The infants will also be followed through one year of age with monthly validated respiratory questionnaires and a follow-up pulmonary function test at 12 months of age. Success of this study is supported by strong pilot data showing statistically significant improvements at about 48 hours of age in pulmonary function tests in infants born to smoking mothers who received vitamin C versus placebo, and preliminary data showing a lower incidence of wheezing at 12 months of age in these infants. Key genetic polymorphisms shown to increase sensitivity to in-utero smoke exposure will also be measured. The success of this study is also supported by animal models showing the effectiveness of vitamin C to preserve pulmonary function and genetic and epidemiologic studies linking the effects of smoking during pregnancy to oxidant mechanisms. The secondary aims of the study include: 1) to demonstrate a decreased incidence of wheezing through 12 months of age in infants delivered to smoking mothers who are randomized to 500mg/day of supplemental vitamin C versus placebo during pregnancy; 2) to demonstrate improved pulmonary function tests at 12 months of age in these infants.

Interventions

DIETARY_SUPPLEMENTVitamin C +prenatal vitamin

Pregnant smoking women will be randomized to daily vitamin C (500 mg) versus daily placebo

DIETARY_SUPPLEMENTPlacebo tablet+prenatal vitamin

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
Office of Dietary Supplements (ODS)
CollaboratorNIH
Oregon Health and Science University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
15 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

At randomization: * Singleton gestation * ≥ 15 years old * Gestational age between 13 and 22 weeks * Receiving prenatal care * Current smoker * English speaking

Exclusion criteria

* Gestational age ≥ 23 and 0/7 weeks * Multiple gestation * Major fetal congenital anomalies * Current use of illicit drugs * Current alcohol abuse * Use of vitamin C (≥ 500 mg/day)\>3 days per week since last menstrual period * Refusal to abstain from vitamin or supplements containing significant vitamin C other than those provided through or approved by study staff * History of kidney stone in patient * Insulin dependent diabetes * Complex maternal medical conditions * Participation in other conflicting research projects * Unable to demonstrate stable method of communication * Pregnancy by in-vitro fertilization * Plan to terminate pregnancy * Failure of medication compliance trial * Failure to return in designated period during placebo run-in * Body mass index \> 50 at screening

Design outcomes

Primary

MeasureTime frameDescription
Forced Expiratory Flow at 75% of Expired Volume (FEF75)3 months of ageThe primary outcome was the comparison of infant FEFs at 3 months of age obtained using the raised volume rapid thoracic compression (RVRTC) technique in offspring of pregnant smokers randomized to vitamin C versus placebo. The specific primary outcome parameter was the measurement of FEF at 75% of the expired volume (FEF75)

Secondary

MeasureTime frameDescription
Forced Expiratory Flow at 75% of Expired Volume (FEF75)12 months of ageThe measurement of forced expiratory flows and specifically FEF75 will be done at 12 months of age in infants born to pregnant smoking women randomized to vitamin C versus placebo during pregnancy. FEF75 will be measured with the raised volume rapid thoracic compression technique.
Incidence of Wheezing Through 12 Months of Age12 months of ageThe incidence of wheezing through 12 months of age will be compared in the infants delivered to smoking pregnant women who were randomized to vitamin C (500 mg) versus placebo during pregnancy.

Countries

United States

Participant flow

Recruitment details

Study staff screened women at prenatal clinics between December, 2012 and June, 2015 in the catchment area of the three clinical sites to identify eligible women who continued to smoke cigarettes.

Pre-assignment details

To exclude highly non-compliant subjects, consented patients entered a medication compliance trial of 14 ± 7 days. Placebo tablets were given to participants and they were excluded if they failed to return for a post compliance visit within 14 ± 7 days of the screening visit or if they took \< 75% of the required tablets.

Participants by arm

ArmCount
Placebo Tablet+Prenatal Vitamin
A daily placebo tablet Placebo tablet+prenatal vitamin
126
Vitamin C +Prenatal Vitamin
Vitamin C +prenatal vitamin: Pregnant smoking women will be randomized to daily vitamin C (500 mg) versus daily placebo
125
Total251

Baseline characteristics

CharacteristicPlacebo Tablet+Prenatal VitaminTotalVitamin C +Prenatal Vitamin
Age, Categorical
<=18 years
10 Participants16 Participants6 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
116 Participants235 Participants119 Participants
Age, Continuous26.4 years
STANDARD_DEVIATION 5.9
26.5 years
STANDARD_DEVIATION 5.6
26.6 years
STANDARD_DEVIATION 5.2
BMI at Enrollment30.0 kg/m^2
STANDARD_DEVIATION 7.3
29.3 kg/m^2
STANDARD_DEVIATION 6.9
28.6 kg/m^2
STANDARD_DEVIATION 6.5
Cigarette Smoking 3 months prior to Pregnancy17.7 cigarettes per day
STANDARD_DEVIATION 10.8
16.8 cigarettes per day
STANDARD_DEVIATION 9.4
15.9 cigarettes per day
STANDARD_DEVIATION 7.7
Cigarette Smoking at Enrollment7.8 cigarettes per day
STANDARD_DEVIATION 4.9
7.9 cigarettes per day
STANDARD_DEVIATION 4.9
8.0 cigarettes per day
STANDARD_DEVIATION 5
Ethnicity (NIH/OMB)
Hispanic or Latino
7 Participants9 Participants2 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
119 Participants241 Participants122 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants1 Participants1 Participants
Gestational Age at Enrollment16.4 weeks
STANDARD_DEVIATION 2.9
16.5 weeks
STANDARD_DEVIATION 3
16.7 weeks
STANDARD_DEVIATION 3.1
Gestational Age at Randomization18.2 weeks
STANDARD_DEVIATION 2.8
18.3 weeks
STANDARD_DEVIATION 2.9
18.4 weeks
STANDARD_DEVIATION 3
Gravida3.5 pregnancies
STANDARD_DEVIATION 2.4
3.4 pregnancies
STANDARD_DEVIATION 2.2
3.3 pregnancies
STANDARD_DEVIATION 2
Health Insurance Type
Government Assistance
106 Participants218 Participants112 Participants
Health Insurance Type
None or Self Pay
2 Participants2 Participants0 Participants
Health Insurance Type
Private Insurance
18 Participants31 Participants13 Participants
Highest Education Level Attained
Bachelor's Degree
6 Participants9 Participants3 Participants
Highest Education Level Attained
Graduate School
0 Participants0 Participants0 Participants
Highest Education Level Attained
High School or GED
40 Participants99 Participants59 Participants
Highest Education Level Attained
Less than High School
31 Participants51 Participants20 Participants
Highest Education Level Attained
Some College
49 Participants92 Participants43 Participants
Marital Status
Divorced
7 Participants15 Participants8 Participants
Marital Status
Married
31 Participants53 Participants22 Participants
Marital Status
Significant Other
39 Participants95 Participants56 Participants
Marital Status
Single
49 Participants88 Participants39 Participants
Maternal History of Alcohol Abuse
No
126 Participants247 Participants121 Participants
Maternal History of Alcohol Abuse
Yes
0 Participants4 Participants4 Participants
Maternal History of Asthma
No
88 Participants169 Participants81 Participants
Maternal History of Asthma
Yes
38 Participants82 Participants44 Participants
Maternal History of Substance Abuse
No
110 Participants215 Participants105 Participants
Maternal History of Substance Abuse
Yes
16 Participants36 Participants20 Participants
Race (NIH/OMB)
American Indian or Alaska Native
2 Participants3 Participants1 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
15 Participants35 Participants20 Participants
Race (NIH/OMB)
More than one race
8 Participants15 Participants7 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
1 Participants1 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
100 Participants197 Participants97 Participants
Region of Enrollment
United States
126 participants251 participants125 participants
Sex: Female, Male
Female
126 Participants251 Participants125 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
1 / 1261 / 1251 / 1231 / 120
other
Total, other adverse events
54 / 12659 / 1250 / 1230 / 120
serious
Total, serious adverse events
30 / 12620 / 12531 / 12333 / 120

Outcome results

Primary

Forced Expiratory Flow at 75% of Expired Volume (FEF75)

The primary outcome was the comparison of infant FEFs at 3 months of age obtained using the raised volume rapid thoracic compression (RVRTC) technique in offspring of pregnant smokers randomized to vitamin C versus placebo. The specific primary outcome parameter was the measurement of FEF at 75% of the expired volume (FEF75)

Time frame: 3 months of age

Population: Population included in analysis were infants who were able to complete technically acceptable PFT/FEF measurements at 3 months of age.

ArmMeasureValue (MEAN)Dispersion
Placebo Tablet+Prenatal VitaminForced Expiratory Flow at 75% of Expired Volume (FEF75)188.7 ml/sStandard Deviation 66.4
Vitamin C +Prenatal VitaminForced Expiratory Flow at 75% of Expired Volume (FEF75)200.7 ml/sStandard Deviation 71.1
Comparison: Our targeted sample size of 218 infants with successful FEFs at 3 months of age was determined to detect with 90% power, at a significance level of 0.05, increases of 15% in mean FEF75 in the vitamin C group compared to the placebo group.p-value: 0.1995% CI: [-6.1, 30.3]ANCOVA
Secondary

Forced Expiratory Flow at 75% of Expired Volume (FEF75)

The measurement of forced expiratory flows and specifically FEF75 will be done at 12 months of age in infants born to pregnant smoking women randomized to vitamin C versus placebo during pregnancy. FEF75 will be measured with the raised volume rapid thoracic compression technique.

Time frame: 12 months of age

Population: These measurements were performed at the 12 month visit.

ArmMeasureValue (MEAN)Dispersion
Placebo Tablet+Prenatal VitaminForced Expiratory Flow at 75% of Expired Volume (FEF75)324 mL/sStandard Deviation 84.1
Vitamin C +Prenatal VitaminForced Expiratory Flow at 75% of Expired Volume (FEF75)351.6 mL/sStandard Deviation 71.1
Secondary

Incidence of Wheezing Through 12 Months of Age

The incidence of wheezing through 12 months of age will be compared in the infants delivered to smoking pregnant women who were randomized to vitamin C (500 mg) versus placebo during pregnancy.

Time frame: 12 months of age

Population: Population is infants who have reached 12 months of age, and whose parent/caregiver has completed at least 1 respiratory questionnaire past 122 days after birth.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Placebo Tablet+Prenatal VitaminIncidence of Wheezing Through 12 Months of Age63 Participants
Vitamin C +Prenatal VitaminIncidence of Wheezing Through 12 Months of Age51 Participants

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026