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Syringe or Continuous Amnioreduction for Symptomatic Polyhydramnios. A Prospective Randomized Study.

NCT00236340 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2025-09-19

No results posted yet for this study

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

Conditions

  • Polyhydramnios

Interventions

DEVICE

Syringe aspiration

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

DEVICE

Wall suction

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

Sponsors & Collaborators

  • Institut National de la Santé Et de la Recherche Médicale, France

    lead OTHER_GOV

Principal Investigators

  • Franck Perrotin, MD PhD · Institut National de la Santé Et de la Recherche Médicale, France

  • Andrea Wagner, MD · Institut National de la Santé Et de la Recherche Médicale, France

  • Gilles Body, MD PhD · CHU Bretonneau TOURS

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-01-31
Primary Completion
2005-02-28
Completion
2005-02-28

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00236340 on ClinicalTrials.gov