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Drotaverine to Shorten the Length of Labor

Primary Purpose

Prolonged First Stage of Labor, Failure of Cervical Dilation as Antepartum Condition, Labor Pain

Status
Completed
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
Drotaverine
Placebo
Sponsored by
Ain Shams Maternity Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prolonged First Stage of Labor

Eligibility Criteria

18 Years - 35 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women aged between 18 and less than 35 years.
  • Primigravidae.
  • Singleton pregnancy.
  • Term gestation i.e., 37-42 weeks.
  • Sure, reliable dates documented by ultrasound in the 1st half of pregnancy.
  • Vertex presentation with occipito anterior position
  • Regular uterine contractions at a rate of at least 3 to 4 contractions every 10 minutes, each contraction lasting for at least 40 seconds.
  • Cervical dilatation of 3-5 cm.
  • With or without rupture of membranes
  • No evidence of maternal or fetal distress.

Exclusion Criteria:

  • Cephalo-pelvic disproportion.
  • Cervical surgery in the past or history of cervical injury.
  • Patients on antihypertensive therapy.
  • Known hypersensitivity to Drotaverine hydrochloride.
  • If any other spasmolytic agent had been used within 48 hours.

Sites / Locations

  • Labor at the delivery unit of Ain Shams Maternity Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Drotaverine

Placebo

Arm Description

Women who will receive 40 mg Drotaverine hydrochloride (Do-Spa) IV injection.

Women who will receive 2ml of normal physiological saline (0.9% sodium chloride) I.V.

Outcomes

Primary Outcome Measures

Duration of the active first stage of labor

Secondary Outcome Measures

Rate of cervical dilation (cm/h)
Effect on pain by using visual analogue scale
Mode of delivery
APGAR score less than 7 at 1 and 5 minutes

Full Information

First Posted
July 9, 2012
Last Updated
January 17, 2013
Sponsor
Ain Shams Maternity Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01639027
Brief Title
Drotaverine to Shorten the Length of Labor
Official Title
Use of Antispasmodic Drotaverine to Shorten the Length of Labor in Nulliparous Women
Study Type
Interventional

2. Study Status

Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
May 2012 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
January 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams Maternity Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Reducing the length of labor is a highly desirable goal of intrapartum care, both from a perspective of maternal and fetal well-being, and for the providers of the birth services. Avoiding along, protracted labor entails shorter exposure to pain, anxiety and stress and would thus translate into a major improvement in maternal satisfaction with the childbirth experience. Based on the premise that shortening the length of labor is beneficial, interventions aimed at accelerating the progression of labor have been introduced routinely as part of standard labor management and care throughout the 20th century. Certain labor accelerative procedures, such as amniotomy, became common practice and have been put to the acid test of randomized control trials to evaluate their efficacy. Use of anticholinergics/antispasmodics as a method of augmenting labor was first described in 1937 by Hirsch, who reported a decrease in labor length by two to four hours following Intrapartum administration of an atropine-like drug (Syntropan®)mainly among older nulliparas. Drotaverine, an isoquinolone derivative is a superior smooth muscle relaxant which acts specifically on spastic sites and corrects the cAMP and calcium balance relieving smooth muscle spasm. This inhibitory action is detected only in lower uterine segment during labor since muscle fibers in upper uterine segment are strongly affected by contractile effect of oxytocin. Use of drotaverine during pregnancy is free of any teratogenic and embryotoxic effects. The Research question is: Does the use of antispasmodic Drotaverine shorten the duration of active first stage of labor in nulliparous women as compared to placebo?
Detailed Description
Research question: Does the use of antispasmodic Drotaverine shorten the duration of active first stage of labor in nulliparous women as compared to placebo? Research hypothesis: the population means of the Drotaverine and placebo groups are equal regarding the duration of the first stage of labor. Objectives: The purpose of this study was to determine the effectiveness of Drotaverine for reducing the duration of labor for the context of contemporary practice, among nulliparous women managed according to a standard intrapartum protocol. Study setting: Patients will be recruited from women admitted in labor at the delivery unit of Ain Shams Maternity Hospital. Study design: This study is a phase II to III, intervention study- Randomized Controlled double blind study. Procedure: Every patient will be subjected to: Complete history to exclude allergy to Drotaverine Hydrochloride and any contraindication for normal vaginal delivery. General examination of the patients including (pulse, blood pressure, temperature). Obstetric Abdominal examination including lie, presentation,station; fetal heart rate, uterine contraction, amount of liquor and to exclude multiple pregnancies. Vaginal examination under aseptic conditions to assess cervical dilation, effacement, state of fetal membranes, presenting part,position of fetal head, color of liquor and pelvic adequacy. Assessment of the frequency, duration of uterine contractions and monitoring of fetal wellbeing will be applied through CTG application on admission: - CTG will be applied half an hour to all participants before starting any intervention. If the contractions are not adequate: Patients with intact membranes → AROM will be done, reassessment after one hour. If still no adequate contraction, Oxytocin infusion will start (five I.U. Oxytocin in 500 cc ringer I.V. drip) by titration method until complete regulation of uterine contractions. Those with ruptured of membranes, the amniotic fluid color will be checked for any abnormalities and Oxytocin infusion will start (five I.U. Oxytocin in 500 cc ringer I.V. drip) by titration method until complete regulation of uterine contractions. If the contractions are adequate: No interference will be done. Each participant will randomly take a prefilled syringe with two milliliters of the study medication solution (either Drotaverine Hydrochloride or saline). Each participant will take the selected syringe slowly intravenously over two minutes. Partographic representation of labor and duration of first stage to determine the primary end point of the study "duration of 1st stage". Cervical effacement and dilatation in addition to station and position of fetal head will be recorded every two hours by vaginal examination. Reassessment after four hours of the first dose: A) If poor progress: Initially, exclude C.P.D. & uterine inertia. If there is an obvious cause: C.P.D.: Urgent C-section will be done. Uterine inertia: adjust the dose of Oxytocin I.V drip via titration method until complete regulation of uterine contraction. If there is no obvious cause: Another dose of the colorless solution will be given then reassessment after four hours, If no progress → re evaluation for final decision of mode of delivery. B) If good progress: No interference will be done. Outcome: Primary outcomes: The duration of the active first stage of labor(Partographic representation for cervical effacement and dilatation will be plotted for each participant). Rate of cervical dilation (cm/h). Secondary outcomes: Effect on pain by using visual analogue scale once before and one hour after injection of solution. VAS will be done at 30, 60 and 120 minutes of the drug administration. Mode of delivery. APGAR score less than 7 at 1 and 5 minutes. Maternal drug side effect will be recorded. Randomization and Blinding: Randomization will be achieved using a computer-generated randomization sequence. Allocation will be in a 1:1 ratio. Records of group allocation will be maintained by a resident physician "other than the researcher" whose responsibility will be randomization and drawing up the injection after dark sealing of the syringes with black opaque stickers to make the yellowish colored Drotaverine Hydrochloride (Do-Spa®) in-differentiable from the translucent saline solution. This house officer has no direct involvement in the intrapartum decision making. Drotaverine Hydrochloride and saline injections will have an identical appearance. The midwives, the clinicians staffing labor and delivery and the patients could not distinguish the placebo from the active drug. The randomization list will be held in a secure box on the labor ward to ensure concealment of the allocation of intervention from those recruiting participants. Data Collection: Maternal characteristics and labor information will be prospectively collected in a computerized database that will be maintained with daily chart review by the researcher to ensure accuracy and to minimize missing data The primary end-point of this study will be the duration of the first stage of labor.The first stage encompasses the onset of active labor to complete cervical dilatation. However, as women will be randomized at different dilatation levels, to allow meaningful comparison the dilatation rates (from administration of study drug o full dilatation) will be calculated and will be used as the primary outcome measure. Analysis: Data analysis and reporting will strictly follow the recommendation of CONSORT 2010 For each primary and secondary outcome, results for each group, and the estimated effect size and its precision (95% confidence interval). For binary outcomes, presentation of both absolute risk difference and relative (Risk Ratio) effect sizes will be reported. Ethical considerations IRB approval: The clinical research study will be conducted in accordance with the current IRB-approved clinical protocol; ICH GCP Guidelines; and relevant policies, requirements, and regulations of the Ain Shams University. Consent procedure: The investigator will make certain that an appropriate informed consent process is in place to ensure that potential research subjects, or their authorized representatives, are fully informed about the nature and objectives of the clinical study, the potential risks and benefits of study participation, and their rights as research subjects. The investigator will obtain written, signed informed consent of each subject, or the subject's authorized representative, prior to performing any study-specific procedures on the subject. The investigator will retain the original signed informed consent form. Subject confidentiality: All laboratory specimens, evaluation forms, reports, video recordings and other records that leave the site will not include unique personal data to maintain subject confidentiality. Funding: Internal funding by using the Hospital resources.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prolonged First Stage of Labor, Failure of Cervical Dilation as Antepartum Condition, Labor Pain, Mild Birth Asphyxia, APGAR 4-7

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
352 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Drotaverine
Arm Type
Active Comparator
Arm Description
Women who will receive 40 mg Drotaverine hydrochloride (Do-Spa) IV injection.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Women who will receive 2ml of normal physiological saline (0.9% sodium chloride) I.V.
Intervention Type
Drug
Intervention Name(s)
Drotaverine
Other Intervention Name(s)
Do Spa
Intervention Description
40 mg Drotaverine hydrochloride (Do-Spa) IV injection at the start of the study and repeated every 2 hours up to a maximum 3 injections.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Normal physiological saline (0.9% sodium chloride)
Intervention Description
Women who will receive 2ml of normal physiological saline (0.9% sodium chloride) I.V at the start of the active phase of labor.
Primary Outcome Measure Information:
Title
Duration of the active first stage of labor
Time Frame
12 hours
Secondary Outcome Measure Information:
Title
Rate of cervical dilation (cm/h)
Time Frame
12 hours
Title
Effect on pain by using visual analogue scale
Time Frame
12 hours
Title
Mode of delivery
Time Frame
12 hours
Title
APGAR score less than 7 at 1 and 5 minutes
Time Frame
12 hours

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women aged between 18 and less than 35 years. Primigravidae. Singleton pregnancy. Term gestation i.e., 37-42 weeks. Sure, reliable dates documented by ultrasound in the 1st half of pregnancy. Vertex presentation with occipito anterior position Regular uterine contractions at a rate of at least 3 to 4 contractions every 10 minutes, each contraction lasting for at least 40 seconds. Cervical dilatation of 3-5 cm. With or without rupture of membranes No evidence of maternal or fetal distress. Exclusion Criteria: Cephalo-pelvic disproportion. Cervical surgery in the past or history of cervical injury. Patients on antihypertensive therapy. Known hypersensitivity to Drotaverine hydrochloride. If any other spasmolytic agent had been used within 48 hours.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mostafa Ibrahem, MD
Organizational Affiliation
Ain Shams University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Mohamed Ellaithy, MD
Organizational Affiliation
Ain Shams University
Official's Role
Study Chair
Facility Information:
Facility Name
Labor at the delivery unit of Ain Shams Maternity Hospital
City
Abbasiya
State/Province
Cairo
ZIP/Postal Code
11566
Country
Egypt

12. IPD Sharing Statement

Citations:
PubMed Identifier
31522581
Citation
Ibrahim MI, Ellaithy MI, Hussein AM, Nematallah MM, Allam HA, Abdelhamid AS, Harara RM, Riad AA, Rafaat TA. Measurement of maternal serum amyloid A as a novel marker of preterm birth. J Matern Fetal Neonatal Med. 2021 Aug;34(15):2467-2472. doi: 10.1080/14767058.2019.1668370. Epub 2019 Sep 25.
Results Reference
derived
PubMed Identifier
24299975
Citation
Ibrahim MI, Alzeeniny HA, Ellaithy MI, Salama AH, Abdellatif MA. Drotaverine to improve progression of labor among nulliparous women. Int J Gynaecol Obstet. 2014 Feb;124(2):112-7. doi: 10.1016/j.ijgo.2013.08.013. Epub 2013 Nov 7.
Results Reference
derived
Links:
URL
http://www.shams.edu.eg/
Description
Ain Shams University

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Drotaverine to Shorten the Length of Labor

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