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Washing the vagina with saline and seeing its effect in labor induced patients

DINOPROSTONE INTRAVAGINAL SLOW RELEASE INSERT FOR LABOUR INDUCTION WITH AND WITHOUT SALINE VAGINAL WASH: A RANDOMISED CONTROLLED TRIAL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/08/027220
Enrollment
164
Registered
2020-08-18
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: O80- Encounter for full-term uncomplicated delivery

Interventions

Intervention1: Vaginal wash with Normal Saline (0.9% Sodium Chloride): Patient will be given vaginal wash With normal saline before dinoprostone vaginal insert for induction of labour. Control Interv

Sponsors

Reshmi S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: singleton pregnancies gestational age of 37 â?? 42 weeks vertex presentation adequate pelvis Bishop score less than 6

Exclusion criteria

Exclusion criteria: pregnant women with ruptured membranes previous uterine scar ante-partum hemorrhage fetal demise major fetal malformations.

Design outcomes

Primary

MeasureTime frame
1.Duration from the beginning of dinoprostone insert vaginally to the active phase of labour (hours) 2. Duration of dinoprostone kept intravaginally (hours) 3. Duration from the time at intravaginal dinoprostone Insertion to full cervical Dilatation (hours)Timepoint: Till the woman goes into active labour(4cm)

Secondary

MeasureTime frame
Change in Bishopâ??s score 2. Mode of delivery-vaginal or Caesarean 3. Indication of Caesarean Section 4. Fetal outcomes including APGAR and birth weight 5. Maternal complications if any 6. Rescue management if any. Timepoint: Till the woman delivers

Countries

India

Contacts

Public ContactReshmi S

Mahatma Gandhi Medical College and Research Institute

rupalsamal@mgmcri.ac.in

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026