Trial · NCT07262242
Effect of Opioid-sparing Anesthesia on Quality of Recovery After Emergency Laparotomy
NCT07262242, Not applicable, Recruiting, Cairo University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effect of Opioid-sparing Anesthesia on Quality of Recovery After Emergency Laparotomy. Trials, record NCT07262242. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07262242
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effect of Opioid-sparing Anesthesia on Quality of Recovery After Emergency Laparotomy
- NCT number
- NCT07262242
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 120 participants, estimated
- Lead sponsor
- Cairo University
- Conditions
- Emergency Abdominal Surgery, Opioid Sparing Anaesthesia
- Interventions
- Lidocaine (drug), Fentanyl (IV)
- First posted
- 2025-12-03
- Last updated
- 2026-10-22
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Quality of recovery using QoR-15 | 24 hours after surgery | The QoR-15 scale is a global measure of postoperative recovery, with a score ranging from 0 (extremely poor QoR) to 150 (excellent QoR) |
| Secondary | intraoperative fentanyl consumption | from time of induction of anesthesia until end of procedure | mcg/kg |
| Secondary | mean arterial pressure | at baseline preoperatively, every 10 minutes (averaging of each 5 readings) from induction of anesthesia until end of procedure, and 2, 6, 10, 16, 24 hours postoperatively. | mmHg |
| Secondary | heart rate | at baseline preoperatively, every 10 minutes (averaging of each 5 readings) from induction of anesthesia until end of procedure, and 2, 6, 10, 16, 24 hours postoperatively. | bpm |
| Secondary | postoperative opioid consumption | from extubation until 24 hours postoperatively | nalbuphine in mg |
| Secondary | numeric rating scale | 30 minutes, 2-, 6-, 10-, 16-, 24 hours postoperatively | rate pain on a scale of 0-10, 0: no pain, 10: worst pain |
| Secondary | serum lactate | 30 minutes postoperative | |
| Secondary | respiratory rate | 30 minutes postoperative | |
| Secondary | Oxygen saturation/ fraction of inspired oxygen (SF ratio) | 30 minutes postoperative |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07262242
GET https://conductscience.org/api/trials/v1/NCT07262242/registered