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Early Oral Intake Following Cesarean Surgery

NCT00370708 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL

Last updated 2006-09-07

No results posted yet for this study

Summary

In this study we are trying to compare the safety and financial benefit of starting the realimentation early versus conventional oral intake following the Cesarean surgery in Iran.

Conditions

  • Obstetrics
  • Surgery

Interventions

PROCEDURE

Oral Intake following admittance to the postpartum ward

Sponsors & Collaborators

  • Tehran University of Medical Sciences

    lead OTHER

Principal Investigators

  • Afsaneh Tehranian, Assist Pro · Department of Obstetrics and Gynecology, Arash Hospital, Tehran University of Medical Sciences, Tehran/Iran

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
20 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2003-04-30
Completion
2004-02-29

Countries

  • Iran

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 NCT00370708 on ClinicalTrials.gov