CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 80 enrolled
Drug / intervention
Syringe aspiration +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00236340
NCT00236340N/ACompleted

DRAINAGE AMNIOTIQUE A LA SERINGUE OU PAR ASPIRATION CONTINUE DANS LES HYDRAMNIOS SYMPTOMATIQUES. ETUDE PROSPECTIVE RANDOMISEE.

Institut National de la Santé Et de la Recherche Médicale, France·interventional·Posted Oct 12, 2005·Updated Sep 19, 2025

In Brief

A clinical study evaluating Syringe aspiration and Wall suction for Polyhydramnios. Completed, enrolled 80 participants across 1 site.

Detailed Summary

To compare the efficiency and maternal and fetal tolerance of two techniques of amnioreduction used in cases of symptomatic second and third trimester polyhydramnios: syringe manual aspiration technique (S group) and continuous suction technique (C group) set to - 250 mmHg

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPolyhydramnios
CountriesFrance
Collaborators--

Timeline

N/ACompletedFinished
20022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedOct 12, 2005
Enrollment StartJan 1, 2002
Primary CompletionFeb 1, 2005
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 20.7 years ago

Interventions

Syringe aspirationdevice

It consists of performing successive aspirations using a 50ml syringe connected to the needle by a flexible tube.

Wall suctiondevice

The tubing is connected to the centralized suction system by continuous vacuum, the value of the applied vacuum is 250mmHg