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Clinical Trials/NCT01546129
NCT01546129UnknownPhase 3

Effect of Dianatal Obstetric Gel (Cross-linked Polyacrylic Acid) on Outcomes in Vaginal Delivery

Rabin Medical Center1 site in 1 country180 target enrollmentStarted: April 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 3
Enrollment
180
Locations
1
Primary Endpoint
Effects on c-section rates

Study Overview

Brief Summary

Perineal massage at the end of labor stage 2 has been investigated in 2 randomized controlled trials using a water soluble lubricant. In one trial a significant reduction of labor stage 2 has been found, both trials did not show a significant increase of perineum integrity.

In the HCB Swiss Study both a significant reduction of labor stage 2 by 30 % as well as a significant increase of perineal integrity have been shown. No adverse events have been reported.

(see also Obstetric gel shortens second stage of labor and prevents perineal trauma in nulliparous women: a randomized controlled trial on labor facilitation. Schaub AF, Litschgi M, Hoesli I, Holzgreve W, Bleul U, Geissbuhler V. J Perinat Med 2008; 36 (2): 129-135).

Today's practice- Lubricants are widely used to enable manual vaginal examination during labor. In Israel midwifes are using Almond Oil for perineal massage at the end of labor stage 2 to protect the perineum. It has been shown for the first time that the use of the Dianatal Obstetric Gel facilitates vaginal childbirth in humans. Dianatal has been introduced to the EU markets in 2008.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Maternal age between 18 and 40 years
  • •signed written informed consent,
  • •intention for vaginal delivery,
  • •nulliparous state or multiparous state
  • •singleton baby in vertex presentation
  • •estimated birth weight between 1500 g and 4500 g
  • •low risk pregnancies at term and late preterm (34 to 42weeks of gestational age)

Exclusion Criteria

  • •contraindications for vaginal delivery
  • •indications for an amnion infection syndrome
  • •suspect for fetal malformations
  • •indications for cephalopelvic disproportion
  • •severe concomitant diseases of the mother

Arms & Interventions

Dianatal Obstetric Gel

Experimental

Standard of care according to the established Guidelines of the Department plus use of Dianatal applied with a vaginal applicator in stage I and stage II of labor

Intervention: Dianatal Obstetric Gel (Cross-linked polyacrylic acid) (Device)

Control

No Intervention

Standard of care according to the established Guidelines of the Department.

Intervention: Dianatal Obstetric Gel (Cross-linked polyacrylic acid) (Device)

Outcomes

Primary Outcomes

Effects on c-section rates

Effects on vaginal operative intervention rates (forceps, vaccum)

Effects on prolonged second stage

Effects on vaginal and Perineum: tears

Effect on episiotomy rate

Effect on labor outcome in premature infants

Secondary Outcomes

  • Effect on labor duration stage 2 (full dilatation of the cervix until delivery of the baby).
  • Effect on labor duration stage 1 (cervical dilatation of uterus between 4 cm and 10 cm, the beginning of stage 1, i.e. 4 cm dilatation should be evaluated as close as possible within routine examination periods)
  • Effect on birth trauma (birth canal lacerations): vaginal lesions, perineal lesions
  • Effect on labor outcomes in state after c-section
  • Effect on pain experience (pain reduction) measured by visual analog scale: use of epidural
  • Effect on postpartum vaginal or urethral burn feeling
  • Effect on newborn outcomes (APGAR score 1, 5 and 10 min after birth; umbilical cord pH; reduction of newborn trauma)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

boris kaplan

Prof. Boris Kaplan

Rabin Medical Center

Study Sites (1)

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