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Efficacy of intravenous glucose-contained fluid in reducing labor duration of pregnant women : A randomized controlled trial

Efficacy of intravenous glucose-contained fluid in reducing labor duration of pregnant women : A randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230605004
Enrollment
164
Registered
2023-06-05
Start date
2023-04-20
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Prolonged labor time Glucose-contained intravenous fluid Obstetric Delivery

Interventions

- Intervention in this research is the glucose component in the intravenous fluid, which we suppose it to be the agent that will provide the power to uterine muscle. Then the uterine smooth muscle wil
Experimental Drug,No Intervention No treatment
Glucose contained intravenous fluid, 0.9%Normal saline

Sponsors

Department of Obstetrics and Gynecology, Sunpasitthiprasong hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1) Single fetal pregnancy which the women age between 18-45 years, and presenting with labor pain at Sunpasitthiprasong hospital. 2) Gestational age between 37 weeks 0 day to 41 weeks 6 days 3) The pregnant women has uterine contraction with cervical so opening between 3-5 cm.

Exclusion criteria

Exclusion criteria: 1) The pregnant women do not want to be the participant. 2) High risk pregnancy, for example - Gestational diabetes mellitus, Overt diabetes mellitus - All type of heart disease - All type of renal disease - All type of liver disease - Pregnancy-induced hypertension, Pre-eclampsia 3) Contraindications for vaginal delivery - Abnormal fetal presentation, for example, breech and transverse presentation. - Fetal macrosomia (definition by estimated fetal weight beyond 4,000 grams) - Inadequated pelvis or Cephalopelvic disproportion. - All type of abnormal placentation, for example, placenta previa or placenta adheren - Previous cesarean section. - History of previous ectopic pregnancy at cornu area, and receive treatment by surgical wedge resection. - Myoma or structural uterine abnormalities that prevent vaginal delivery. 4) Fetal abnormalities, for example, Non-reassuring fetal status, fetal anomalies, and death fetus in utero.

Design outcomes

Primary

MeasureTime frame
Total labor time From the onset of true labor pain to the onset of fully dilatation of cervix Record the duration of the active phase of first stage and second stage of the labor in minutes

Secondary

MeasureTime frame
Latent phase of first stage of labor The duration from the onset of true labor pain to the time that cervix open 3-5 cm. Record the duration of latent phase of first stage of labor,Active phase of first stage of labor The duration from the time that cervix open 3-5 cm. to the onset of fully dilatation Record the duration of active phase of first stage of labor,First stage of labor The duration from the onset of true labor pain to the onset of fully dilatation Record the duration of latent and active phase of first stage of labor,Second stage of labor The duration from the onset of fully dilatation to placental delivery Record the duration of second stage of labor,Third stage of labor The duration from the onset of fully dilatation to placental delivery Record the duration of third stage of labor,Prolonged latent phase The duration of latent phase that exceed 8 hours Record the duration of latent phase. If the duration of latent phase exceed 8 hours that means prolonged latent phase,Augmentation duration The duration that the participants receive oxytocin administration Record the duration that the participants receive oxytocin administration,Total fluid volume The total volume that each participant received since she admitted to the labor room Record the volume of intravenous fluid that the participants received,Route of delivery The time that the participant gave birth Record route of delivery of each participant,Intrapartum complication During labor periods, which include the first, second, and third stage of labor Record the complications which occur during labor period, for example, fetal distress, shoulder dystocia, and failed vacuum extraction.,Postpartum complications After fetal delivery Record the complications which occur after fetal delivery, for example, postpartum hemorrhage, fourth degree perineum tear, and perineum hematoma ,Birth body weight The time after fetal delivery Record the body weight of neonate after delivery,Apgar score At 1,5,10 minute

Countries

Thailand

Contacts

Public ContactWanatchaporn Puttakul

Department of Obstetrics and Gynecology, Sunpasitthiprasong hospital

Wanatchaporn1012@gmail.com0836163329

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026