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Efficacy of Ginger in the Prevention of Abdominal Distention in Post Cesarean Section Patient

NCT02809027 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 178

Last updated 2020-07-15

No results posted yet for this study

Summary

The purpose of this study is to determine ginger is effective in the prevention of abdominal distention in post Cesarean section patient.

Conditions

  • Post Cesarean Section Patient

Interventions

DRUG

Ginger

DRUG

Placebo

Sponsors & Collaborators

  • Chulalongkorn University

    lead OTHER

Principal Investigators

  • Vorapong Phupong, M.D. · Chulalongkorn University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-06-01
Primary Completion
2017-06-30
Completion
2017-06-30

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Drugs

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 NCT02809027 on ClinicalTrials.gov