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Oral Intake During Labor

NCT03276741 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 126

Last updated 2020-04-24

No results posted yet for this study

Summary

A randomized clinical trial (RCT) to evaluate the impact of unrestricted low fat, low residue oral intake during labor on maternal and neonatal outcomes as well as maternal satisfaction.

Conditions

  • Labor Complication
  • Food Aspiration
  • Complication of Anesthesia
  • Satisfaction

Interventions

DIETARY_SUPPLEMENT

gastric soft/bland diet

Patients in the experimental group will have a gastric soft/bland diet available.

Sponsors & Collaborators

  • David Grant U.S. Air Force Medical Center

    lead FED

Principal Investigators

  • Jeanette M Anderson, MSN · David Grant Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-09-29
Primary Completion
2020-01-11
Completion
2020-01-11

Countries

  • United States

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 NCT03276741 on ClinicalTrials.gov