NCT03050684 is a NA clinical trial of vaginal lavage group in Labor Induction, sponsored by Zeynep Kamil Maternity and Pediatric Research and Training Hospital.

Who is sponsoring NCT03050684?

NCT03050684 is sponsored by Zeynep Kamil Maternity and Pediatric Research and Training Hospital.

What drugs are being tested in NCT03050684?

Interventions in NCT03050684: vaginal lavage group, Control Group.

What condition does NCT03050684 study?

NCT03050684 studies Labor Induction, Dinoprostone Vaginal Insert, Vaginal Infection, Effect Increased.

Is NCT03050684 still recruiting?

NCT03050684 is currently completed. Last updated 31 January 2018.

Last reviewed 2018-01-31 · How we verify

NCT03050684

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

Does Vaginal Washing Affect the Success Rate of the Labour Induction?

Completed NA Last updated 31 January 2018

What this trial tests

NA trial testing vaginal lavage group in Labor Induction in 200 participants. Completed in 20 December 2017.

Timeline

20 February 2017

Primary endpoint
10 December 2017

20 December 2017

Quick facts

Lead sponsor	Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Phase	NA
Status	Completed
Study type	INTERVENTIONAL
Allocation	randomized
Design	parallel
Masking	quadruple
Primary purpose	screening
Enrollment	200
Start date	20 February 2017
Primary completion	10 December 2017
Estimated completion	20 December 2017
Sites	1 location across Turkey (Türkiye)

Drugs / interventions tested

vaginal lavage group
Control Group — full drug profile →

Conditions studied

Labor Induction — all drugs for Labor Induction →
Dinoprostone Vaginal Insert — all drugs for Dinoprostone Vaginal Insert →
Vaginal Infection — all drugs for Vaginal Infection →
Effect Increased — all drugs for Effect Increased →

Sponsor

Zeynep Kamil Maternity and Pediatric Research and Training Hospital

Who can join

Adults 18 to 40, female only, with Labor Induction or Dinoprostone Vaginal Insert. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Investigators will use dinoprostone(Propess TM) for cervix ripening and labor induction in term pregnant women.Vaginal pH base is achieved with the effect of hormones in pregnancy and associated with this, vaginal infections rates increase. With the vaginal application of Propess, the preparate remains in the vagina for a long time, with controlled release,creating a film layer against bacteria and especially fungal infections and it was thought that this could be a reason for unsuccessful birth induction by preventing release of this ovule. The aim of this study is to observe whether or not the rate of caesareans with the indication of unsuccessful induction was reduced in patients by reducing the density of vaginal bacteria and fungi with vaginal lavage and thereby increasing the effect of the drug and decreasing the rate of unsuccessful inductions.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Labor Induction

Currently open trials in the same condition.

NCT07006896 — Induction of Labor After Cesarean Using Foley Alone vs. Concurrent Foley and Oxytocin · NA · recruiting
NCT07109258 — Effect of Dexamethasone on Labour Induction in Term Pregnancies · EARLY_PHASE1 · recruiting

Other Zeynep Kamil Maternity and Pediatric Research and Training Hospital trials

Trials by the same sponsor.

NCT05786352 — Outcomes of Enhanced Recovery After Cesarean (ERAC) Protocol · NA · unknown
NCT07312617 — Short-Term Outcomes of TOT, TVT, and Burch Surgery Assessed by Transperineal Ultrasound · NA · completed
NCT05558046 — Predictive Value of Granulosa Cell DNA Damage in the Success of Assisted Reproductive Technique · unknown
NCT05558852 — Laparoscopic Central and Anterior Compartment Prolapse Surgery: A Meshless Sacrocolpopexy Technique · NA · unknown
NCT04888091 — Comparison of the Effect of Cervical Mucus Cleaning Method Applied Before Embryo Transfer on Pregnancy Rates. · NA · completed

Verify against primary sources

ClinicalTrials.gov — authoritative US registry record
WHO ICTRP — international registry index
EU Clinical Trials Register
Sponsor press releases (Google)

Data sources for this page

Trial protocol + status: ClinicalTrials.gov NCT03050684 (US National Library of Medicine, public domain)
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Last refreshed: 31 January 2018

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03050684.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing