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

Phase 2

Recruiting

• Conditions: Prolonged labor time Glucose-contained intravenous fluid; Obstetric Delivery

• Registration Number: TCTR20230605004
• Lead Sponsor: Department of Obstetrics and Gynecology, Sunpasitthiprasong hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-06-05
• Study Completion: 2023-09-18
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 160

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

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.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of labor From the onset of true labor pain until fetal and placental delivery Measure and record all stage of the labor time in minutes, from the onset of true labor pain to the time which fetal and placental delivery.

Secondary Outcome Measures

Name	Time	Method
Neonatal outcome The first 10 minutes after the fetal delivery, which we evaluate the APGAR score. Record the fetal APGAR score,Maternal outcome From the time which the mother delivery to the time before the mother discharge from the hospital (normally 3 days) Number of events of maternal complications, for example, post-partum hemorrhage, infected episiotomy wound, and maternal fever.