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Prospective, Double Blind, Placebo Control, Bariatric IV Ace

Prospective, Double Blind, Placebo Control, Study of Acetaminophen iv on Hospital Length of Stay in Morbidly Obese Individuals Undergoing Elective Laparoscopic Sleeve Gastrectomy

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02452320
Acronym
Bariatricace
Enrollment
136
Registered
2015-05-22
Start date
2016-02-29
Completion date
2017-01-31
Last updated
2018-04-20

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

Conditions

Obesity

Keywords

bariatric, Post-operative nausea and vomiting, laparoscopic Sleeve gastrectomy, intravenous acetaminophen

Brief summary

The purpose of this study is to determine if the administration of acetaminophen given intravenously (through an IV) beginning during surgery and then for 3 additional doses during the first 24 hours post-operatively will reduce the length of time subjects undergoing elective sleeve gastrectomy spend in the hospital following this operation. Additional questions that may be answered include whether administration of the study medication leads to improvement in pain control, a reduction in post-operative nausea and vomiting, and an overall improvement in quality of recovery.

Detailed description

Morbid obesity is defined as a body mass index (BMI: weight \[kg\] / height \[m\]2) ≥ 40 or ≥ 35 if associated with comorbidities, and it is widely prevalent, nationally and globally. Overweight or obese individuals have increased morbidity and mortality. Among the many available treatment options, surgical management of obesity has been shown to be the most reliably effective in achieving sustained weight loss and improvements in glycemic, lipidemic, and blood pressure control, and improves five and ten year survival in contrast to matched controls who did not have surgery. Various surgical approaches have been used to provide long-term control of morbid obesity and its associated comorbidities, including laparoscopic sleeve gastrectomy. During a sleeve gastrectomy the greater curvature of the stomach is separated from the lesser curvature and antrum, thereby eliminating \ 85% of the total stomach, including the grehlin-producing portion of the stomach. A common complication of the procedure is postoperative nausea and vomiting (PONV), occurring in nearly 80% of patients undergoing the procedure. Risk factors for PONV include: female sex, history of PONV or motion sickness, nonsmoking, younger age, general vs. regional anesthesia, use of volatile anesthetics and nitrous oxide, administration of postoperative opioids, duration of anesthesia, and type of surgery (including cholecystectomy, laparoscopic, and gynecological). At the individual level, PONV adversely impacts both patient satisfaction and quality of life scores. At the systems level, PONV is associated with increased length of stay (LOS) in the post-anesthesia care unit and hospital, and can result in increased costs. Both pharmacological and surgical approaches have been studied in an effort to reduce the incidence of PONV in sleeve gastrectomy patients. Omentopexy was unsuccessful, and pharmacologic prophylaxis with two \[dexamethasone + odansetron; dexamethasone + granisetron; aprepitant + odansetron; or three (dexamethasone + odansetron + haloperidol; antiemetic agents was more effective than a single agent (odansetron or granisetron) alone in decreasing both nausea and vomiting. Even with triple therapy, just over 50% of patients were nauseous and 20% vomited within the first 36 hours following surgery, and hospital LOS was unaffected. Thus, there is a pressing need for improved control of PONV in sleeve gastrectomy patients. Acetaminophen (N-(4-hydroxyphenyl)acetamide; paracetamol) is a mild analgesic whose main, but not sole, mechanism of action is thought to arise from inhibition of the cyclooxygenase pathway; the intravenous (iv) formulation (acetaminophen iv; ACP-iv) received US Food and Drug Administration (FDA) approval in November 2010 but has been available in Europe since 2002. It is approved by the FDA for the management of mild to moderate pain as a single agent and the management of moderate to severe pain with adjunctive opioid analgesics. Recently, two meta-analyses have evaluated the use of ACP-iv in the postoperative period for its efficacy in preventing postoperative pain \[45\] or reducing PONV \[46\]. In the study by De Oliveria et al., ACP-iv administration was found to significantly reduce postoperative pain, opioid consumption, and PONV. Similarly, the study by Apfel and colleagues indicated that iv-ACP, when administered prophylactically, reduced PONV as a consequence of improved pain control. With direct relevance to sleeve gastrectomy patients, a retrospective analysis of patients undergoing bariatric surgery (sleeve gastrectomy or laparoscopic Roux-en-Y gastric bypass) found that ACP-iv administration reduced opiate consumption and hospital LOS. The investigators hypothesize that administration of ACP-iv in the perioperative period will reduce hospital LOS in sleeve gastrectomy subjects and will be associated with a reduction in hospital costs. The secondary hypothesis is that administration of ACP-iv will reduce PONV and improve subject satisfaction scores in the same subject population.

Interventions

administration of 1000mg of intravenous acetaminophen or placebo every 6 hours for a total of 4 doses; first dose to be administered after induction of general anesthesia

DRUGPlacebo

Subjects randomized to placebo will receive every 6 hours for a total of 4 doses; first dose to be administered after induction of general anesthesia

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* At least 18 years old * BMI \> 30 * Undergoing Elective Sleeve Gastrectomy * Able to consent

Exclusion criteria

* Allergy/ Hypersensitive to acetaminophen or formulation incipients * Allergy/Hypersensitive to aprepitant, ondasteron (serotonin type 3 receptor antagonists), dexamethasone * Allergy to Propofol or formulation incipients (egg albumin, soy lecithin) * Diagnosis or positive family history of malignant hyperthermia * Abnormal LFTs (AST and ALT) \>2x local upper limits of normal * Renal impairment (creatinine clearance (CrCl) ≤ 30mL/min adjusted for obesity)) * Pregnancy * Alcohol consumption \> 3 drinks/day * Requires awake intubation * Unable to provide consent

Design outcomes

Primary

MeasureTime frameDescription
Quality of Recovery-15 Patient SurveyPatients will be followed for the duration of hospital stay, expected average of 3 days.Survey asking 15 questions with regard to how the patient is feeling scored on a scale from 0-10, with 0 being none of the time and 10 being all of the time. Possible scores range from 0-150, and scores with a higher value indicate a better outcome. Each subject was administered a baselineQoR-15 survey prior to surgery, and then one on postoperative days (POD) 1 and 2. If a subject was discharged prior to POD2, they were not given a QoR-15 survey that day.

Secondary

MeasureTime frameDescription
Length of Hospital StayParticipants will be followed for the duration of hospital stay, expected average of 3 days.Monitoring the length of hospital stay after undergoing surgery
Hospital CostsCosts incurred during hospital stay, expected average of 3 days.Accessing billing codes/hospital costs for each enrolled subject from the time they are admitted until they are discharged from the hospital.

Countries

United States

Participant flow

Pre-assignment details

136 subjects were informed of and consented to participate. Due to unforeseen scheduling conflicts and canceled surgeries, we recruited more subjects in order to reach our 128 recruitment mark for statistical analysis. 1 subject was not included in the analysis due to a prolonged hospitalization not related to the study.

Participants by arm

ArmCount
Placebo
Subjects randomized into the control group will not receive study medication, they will receive a placebo administered at the same schedule as the active drug in the other arm. Placebo: Subjects randomized to placebo will receive every 6 hours for a total of 4 doses; first dose to be administered after induction of general anesthesia
64
Acetaminophen IV
Subjects randomized into the active treatment group will receive intravenous acetaminophen intravenous acetaminophen: administration of 1000mg of intravenous acetaminophen or placebo every 6 hours for a total of 4 doses; first dose to be administered after induction of general anesthesia
63
Total127

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyAdverse Event01

Baseline characteristics

CharacteristicPlaceboAcetaminophen IVTotal
Age, Continuous39.1 years
STANDARD_DEVIATION 12.2
42.2 years
STANDARD_DEVIATION 12.2
40.7 years
STANDARD_DEVIATION 12.2
BMI47.3 kg/m^2
STANDARD_DEVIATION 7.9
46.6 kg/m^2
STANDARD_DEVIATION 7.7
46.9 kg/m^2
STANDARD_DEVIATION 7.8
Height (cm)164.8 cm
STANDARD_DEVIATION 10.8
165.5 cm
STANDARD_DEVIATION 9.2
165.2 cm
STANDARD_DEVIATION 10
Race/Ethnicity, Customized
Black or African American
20 Participants16 Participants36 Participants
Race/Ethnicity, Customized
More than one race
7 Participants13 Participants20 Participants
Race/Ethnicity, Customized
Unknown or Not Reported
13 Participants13 Participants26 Participants
Race/Ethnicity, Customized
White
24 Participants21 Participants45 Participants
Region of Enrollment
United States
64 participants63 participants127 participants
Sex: Female, Male
Female
47 Participants45 Participants92 Participants
Sex: Female, Male
Male
17 Participants18 Participants35 Participants
Weight (kg)130 kg
STANDARD_DEVIATION 27.1
127.5 kg
STANDARD_DEVIATION 25.4
128.8 kg
STANDARD_DEVIATION 26.3

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 640 / 63
other
Total, other adverse events
0 / 640 / 63
serious
Total, serious adverse events
0 / 641 / 63

Outcome results

Primary

Quality of Recovery-15 Patient Survey

Survey asking 15 questions with regard to how the patient is feeling scored on a scale from 0-10, with 0 being none of the time and 10 being all of the time. Possible scores range from 0-150, and scores with a higher value indicate a better outcome. Each subject was administered a baselineQoR-15 survey prior to surgery, and then one on postoperative days (POD) 1 and 2. If a subject was discharged prior to POD2, they were not given a QoR-15 survey that day.

Time frame: Patients will be followed for the duration of hospital stay, expected average of 3 days.

Population: Subjects were administered a QoR-15 Survey pre-operatively as a baseline, and on post-operative days 1 and 2. Some subjects were discharged prior to the administration of the QoR-15 on post-operative day 2 and therefore there is no data for those subjects that we no longer in the hospital.

ArmMeasureGroupValue (MEAN)Dispersion
PlaceboQuality of Recovery-15 Patient SurveyPOD 1107.2 units on a scaleStandard Deviation 18.8
PlaceboQuality of Recovery-15 Patient SurveyPOD 2118.3 units on a scaleStandard Deviation 17.3
Acetaminophen IVQuality of Recovery-15 Patient SurveyPOD 1108.6 units on a scaleStandard Deviation 20.9
Acetaminophen IVQuality of Recovery-15 Patient SurveyPOD 2117.1 units on a scaleStandard Deviation 21.1
p-value: 0.59t-test, 2 sided
Secondary

Hospital Costs

Accessing billing codes/hospital costs for each enrolled subject from the time they are admitted until they are discharged from the hospital.

Time frame: Costs incurred during hospital stay, expected average of 3 days.

Population: Used the Hospital cost data for the subjects enrolled in both arms of the study for the duration of their hospitalization.

ArmMeasureValue (MEDIAN)
PlaceboHospital Costs12,977 Dollars (USD)
Acetaminophen IVHospital Costs12,885 Dollars (USD)
Secondary

Length of Hospital Stay

Monitoring the length of hospital stay after undergoing surgery

Time frame: Participants will be followed for the duration of hospital stay, expected average of 3 days.

Population: Subjects LoS were recorded from time of PACU admission till time that Discharge Orders were completed.

ArmMeasureValue (MEDIAN)
PlaceboLength of Hospital Stay1.96 days
Acetaminophen IVLength of Hospital Stay1.87 days

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026