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Early Oral Intake Following Cesarean Surgery

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00370708
First Posted: September 1, 2006
Last Update Posted: July 25, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Tehran University of Medical Sciences
  Purpose
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.

Condition Intervention
Obstetrics Surgery Procedure: Oral Intake following admittance to the postpartum ward

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Single
Primary Purpose: Supportive Care
Official Title: Early Oral Intake Following Elective Cesarean Surgery in Iranian Women; the Economic Burdens and Patient Satisfaction

Further study details as provided by Tehran University of Medical Sciences:

Primary Outcome Measures:
  • Tolerance of Oral Intake

Study Start Date: April 2003
Estimated Study Completion Date: February 2004
Detailed Description:
Cesarean delivery is announced to constitute 50% of deliveries in the Capital and 39% of all the deliveries nationwide, which is far beyond the acceptable international normal range, according to the official site of the Ministry of Health and Medical Education of the Islamic Republic of Iran [http://www.mohme.gov.ir/HNDC/Indicators/Simaye_Salamt/Simaye_Salamat.htm]. This high rate of elective cesarean deliveries might be due to several reasons which are far beyond the scope of this study. Here we tried to see whether the reduction in the time of hospitalization for these patients is safe at the expense of earlier oral realimentation and to see whether this strategy increases the patients' satisfaction or not.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 35 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

Women who had elective cesarean deliveries under regional anesthesia

Exclusion Criteria:

  1. Receiving general anesthesia, magnesium sulfate or insulin.
  2. Coming across an intraoperative bowel injury.
  3. Having any medical or gastrointestinal problem that prohibits early feeding
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00370708


Locations
Iran, Islamic Republic of
Department of Obstetrics and Gynecology, Arash Hospital
Tehran, Iran, Islamic Republic of, 19986
Sponsors and Collaborators
Tehran University of Medical Sciences
Investigators
Principal Investigator: Afsaneh Tehranian, Assist Pro Department of Obstetrics and Gynecology, Arash Hospital, Tehran University of Medical Sciences, Tehran/Iran
  More Information

ClinicalTrials.gov Identifier: NCT00370708     History of Changes
Other Study ID Numbers: 1383FK
First Submitted: August 31, 2006
First Posted: September 1, 2006
Last Update Posted: July 25, 2007
Last Verified: April 2004

Keywords provided by Tehran University of Medical Sciences:
Cesarean
Oral
Intake