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Status unknownNCT05290753Updated May 3, 2022

Impact of Prokinetic Use After Emergency Intestinal Anastomosis on Postoperative Clinical Outcomes

An interventional study of Prokinetic Motility Agents as primpiram and gastreg in Prokinetic Use After Emergency Intestinal Anastomosis, sponsored by Sohag University. Status unknown at 1 site in Egypt. Open to participants aged 12 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-05-03.

Sponsored by Sohag University · Not applicable, Interventional, and Other

The sponsor has not verified this record recently (last verified Apr 2022), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
15
Allocation
Not applicable
Ages
12 Years and older
Sex
All
01

Study summary

Prokinetic drugs used to accelerate healing of intestinal anastomosis of urgent cases which not prepared preoperative by increase intestinal motility and gastric emptying and decrease postoperative adhesions They are many types of prokinetics as cholinergic agonists, dopamine antagonist, serotonergic agonists and macrolides Agents of prokinetics administered immediately post operation and at the time of hospitalization

Read the detailed description

By evaluation the effect of prokinetic use versus non use after emergency intestinal intestinal anastomosis on short and long term clinical outcome It will be prospective cohort study which conducted in sohag university hospital Study will include patients presented with urgent anastomosis Inclusion criteria: all adults underwent emergency intestinal anastomosis Exclusion criteria: pediatrics, patients with comorbidities and patients with electively resection and anastomosis.

Primary goals are to detect effect of prokinetics on incidence of leakage rate Secondary outcomes include early bowel opening, enteral feeding, post operative pain, wound infection and adhesion formation rate.

02

Conditions studied

  • Prokinetic Use After Emergency Intestinal Anastomosis

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03

In context

Emergencies

1,692 studies on the registry are indexed under Emergencies; 333 are open to participants now.

This study's planned enrollment of 15 is below the median of 145 across 931 interventional studies indexed under Emergencies.

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Lead sponsor

Sohag University is the lead sponsor of 1,183 studies on the registry; 612 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • all adult patients

Exclusion criteria

Exclusion Criteria:

  • pediatrics
  • patients associated with comorbidities
  • patients with electively resection and anastomosis
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
15 participants (estimated)

Study arms

  • Other
    Prokinetic use in accelerate healing of urgent intestinal anastomosis

    Prikinetic agents administered immediately post operative and time of stay at hospital twice daily

    Drug: Prokinetic Motility Agents as primpiram and gastreg

Interventions

  • DrugProkinetic Motility Agents as primpiram and gastreg

    Prospective cohort study to evaluate the effect of pro kinetic use in emergency intestinal anastomosis

    Also known as: Primpiram and gastreg and erythromycin

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What researchers measure

Primary outcomes

  1. Leakage rate

    Fecal fistula

    Time frame: 5 days postoperative

Secondary outcomes

  1. Early bowel opening

    Duration taken to patient to pass feces and flatus

    Time frame: 3 days postoperative

07

Study locations

1 site
  • Of medicine, Sohag university hospital
    Sohag, Egypt
08

References and documents

Publications

  • Acosta A, Camilleri M. Prokinetics in gastroparesis. Gastroenterol Clin North Am. 2015 Mar;44(1):97-111. doi: 10.1016/j.gtc.2014.11.008. Epub 2014 Dec 23. PubMed 25667026 ↗

Individual participant data

Plan to share: Yes — Evaluate the use of prokinetic versus non use in emergency intestinal anastomosis

Supporting information: Study protocol

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 3, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05290753
Lead sponsor
Sohag University
Responsible party
Doha Adel Noureldin (Resident doctor at general surgery department sohag university hospital, Sohag University) — Principal investigator
First posted
Mar 22, 2022
Start date
Jan 1, 2022
Primary completion
Jun 1, 2022 (estimated)
Completion
Jul 1, 2022 (estimated)
Last update
May 3, 2022

Study contacts

Alaa eldin Hassan, Professor
study director · Professor of general surgery

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2022. You cannot join it, but the record below documents what was studied.

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