Trial · NCT07903389
Comparison of Ciprofol, Remimazolam and Propofol in Laparoscopic Colorectal Surgery
NCT07903389, Not applicable, Completed, The First Affiliated Hospital of Zhengzhou University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparison of Ciprofol, Remimazolam and Propofol in Laparoscopic Colorectal Surgery. Trials, record NCT07903389. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07903389
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparison of Ciprofol, Remimazolam and Propofol in Laparoscopic Colorectal Surgery
- NCT number
- NCT07903389
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 180 participants, actual
- Lead sponsor
- The First Affiliated Hospital of Zhengzhou University
- Conditions
- Colorectal Diseases Undergoing Elective Laparoscopic Colorectal Surgery
- Interventions
- Ciprofol, Remimazolam, Propofol
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Postoperative Quality of Recovery Scale-15 (QoR-15) score | Postoperative day 1 | QoR-15 consists of 15 items covering 5 domains: pain, physical comfort, emotional state, psychological support, and physical independence. Total score ranges from 0 to 150; higher score indicates better postoperative recovery. Assessed at postoperative day 1. |
| Secondary | Mean arterial pressure (MAP) | Before anesthesia induction, After tracheal intubation, 30 minutes after surgical incision, At the end of surgery, At extubation | Description: Mean arterial pressure measured during perioperative period |
| Secondary | Cough Visual Analogue Scale (VAS) pain score | 6, 12, 24, and 48 hours after surgery | Cough-induced visual analogue scale (VAS) pain scores were assessed at 6 hours, 12 hours, 24 hours, and 48 hours postoperatively. Cumulative opioid consumption was recorded at 24 hours and 48 hours after surgery. The VAS score ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. |
| Secondary | Perioperative adverse events | From anesthesia induction to 48 hours postoperatively | Incidence of hypotension, bradycardia, postoperative nausea and vomiting, respiratory depression, delayed emergence, postoperative delirium. |
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.
Papers2
The papers the trial lists on ClinicalTrials.gov.
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/NCT07903389
GET https://conductscience.org/api/trials/v1/NCT07903389/registered