Early Oral Feeding Versus Traditional Delayed Oral Feeding Post-perforated Peptic Ulcer Repair

Sponsor
Cairo University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06042933
Collaborator
(none)
120
1
2
7
17.1

Study Details

Study Description

Brief Summary

This study aims to evaluate safety and benefits of early oral feeding compared to traditional delayed oral feeding in patients undergoing perforated peptic ulcer repairs. Study population & Sample size :(

Condition or Disease Intervention/Treatment Phase
  • Other: Post operative early oral feeding
  • Other: Traditional delayed oral Feeding Post-perforated Peptic Ulcer Repairs
N/A

Detailed Description

Study Design:

This study is a single-center, prospective, parallel arm, randomized controlled trial. Patients will be randomly assigned in 1:1 ratio to receive either delayed oral feeding or early oral feeding.

Methods:

Patients will be randomly assigned into two groups. Group A patients followed an early oral feeding protocol(12 hours), and Group B received delayed oral feeding (72 hours).

Outcome parameter :

The outcomes are incidence of postoperative complications including Postoperative repair leakage, Infection-related postoperative complications , Number of days of hospital stay and return of bowel function and Diet intolerance.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized controlled trialRandomized controlled trial
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Early Oral Feeding Versus Traditional Delayed Oral Feeding Post-perforated Peptic Ulcer Repair: A Comparative Study in Egyptian Tertiary Health Care Center
Actual Study Start Date :
Mar 2, 2023
Anticipated Primary Completion Date :
Sep 25, 2023
Anticipated Study Completion Date :
Oct 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group A

early oral intake 6 hours postoperative.

Other: Post operative early oral feeding
To start oral feeding 6 hours after perforated peptic ulcer repairs

Active Comparator: Group B

delayed oral intake after 72 hours

Other: Traditional delayed oral Feeding Post-perforated Peptic Ulcer Repairs
To start oral feeding after 48 hours

Outcome Measures

Primary Outcome Measures

  1. number of days of hospital stay [Up to 10 days]

    number of days of hospital stay

  2. days needed for frist Bowel motion [7 days]

    number of days before frist bowel motion

Secondary Outcome Measures

  1. incidence of Post operative repair leak [30 days]

    number of Post operative repair leaks

  2. severity of operative pain measured by Visual Analogue Scale (VAS) [7 days]

    from 1 to 10 1 indicated minimum pain and 10 maximum pain

  3. INCIDENCE OF postoperative nausea and vomiting (PONAV) [7 days]

    number of cases with postoperative nausea and vomiting (PONAV)

  4. incidence of Surgical site infection [30 days]

    number of cases complicated with surgical site infection

  5. incidence of Pulmonary complications [30 days]

    number of cases complicated Pulmonary complications

  6. incidence of Ryle reinsertion [7 days]

    number of cases complicated Ryle reinsertion

  7. number of Readmission cases [30 days]

    number of cases complicated Readmission cases

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All consecutive patients, of age 18 years and above, who were

presented to the emergency surgical team and were diagnosed with perforated duodenal ulcer by surgicalteam, were recruited and assessed for eligibility.

Exclusion Criteria:
  • • Preoperative refractory septic shock on admission.

  • Delayed presentation more than 24 hours.

  • The presence of neuropsychiatric disease, pregnant and lactating women.

  • Predisposing factors for impaired wound healing (e.g., currently using immunosuppressive agents, or chronic use of steroids), the presence of HIV.

  • American society of anesthesiologists grade iii/iv, or had an alternative perioperative diagnosis.

  • Intraoperatively, after randomization, patients were excluded based on the following criteria: perforated duodenal ulcer ≥20 mm, consistent with malignant ulcers.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cairo University Cairo Egypt 11511

Sponsors and Collaborators

  • Cairo University

Investigators

  • Principal Investigator: mohammed elshwadfy, Cairo University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mohammed Elshwadfy Nageeb, lecturer of general surgery, Cairo University
ClinicalTrials.gov Identifier:
NCT06042933
Other Study ID Numbers:
  • N-96-2023
First Posted:
Sep 21, 2023
Last Update Posted:
Sep 21, 2023
Last Verified:
Sep 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 21, 2023