Trial · NCT07584902
A 2×2 Factorial Randomized Controlled Trial for ERCP
NCT07584902, Not applicable, Not yet recruiting, Gang Chen
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. A 2×2 Factorial Randomized Controlled Trial for ERCP. Trials, record NCT07584902. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07584902
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- A 2×2 Factorial Randomized Controlled Trial for ERCP
- NCT number
- NCT07584902
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 236 participants, estimated
- Lead sponsor
- Gang Chen
- Conditions
- Biliary and Pancreatic Diseases, Endoscopic Retrograde Cholangiopancreatography (ERCP)
- Interventions
- Anesthesia induction using propofol+sufentanil, Anesthesia induction using propofol+esketamine, Anesthesia induction using ciprofol+sufentanil, Anesthesia induction using ciprofol+es-ketamine
- First posted
- 2026-05-13
- Last updated
- 2026-05-13
Source ClinicalTrials.gov
Registered outcomes16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | hypoxemia | perioperative | SpO2≤92% |
| Primary | Hypotension | Perioperative | blood pressure drop exceeding 20% of the baseline value, with mean arterial pressure ≤65 mmHg or systolic blood pressure ≤90 mmHg |
| Secondary | Severe hypoxemia | Perioperative | 75% ≤ SpO2\<90%\>60 s, SpO2\<75%. |
| Secondary | Hypotension/hypertension requiring the use of vasopressors. | Perioperative | Hypotension/hypertension requiring the use of vasopressors. |
| Secondary | Body movement. | Perioperative | During ERCP, the patient's body movement affected the surgical procedure |
| Secondary | Coughing | Perioperative | During ERCP, the patient experienced coughing, which affected the surgical progress |
| Secondary | Hiccup | Perioperative | During ERCP, the patient experienced Hiccup, which affected the surgical progress。 |
| Secondary | Need to urgently switch to endotracheal intubation or interrupt ERCP process due to airway operation | Perioperative | Need to urgently switch to endotracheal intubation or interrupt ERCP process due to airway operation |
| Secondary | Tachycardia (>100 beats/minute) or bradycardia (<50 beats/minute). | Perioperative | Tachycardia (HR\>100 beats/minute) or bradycardia (HR\<50 beats/minute). |
| Secondary | The dosage of remifentanil used. | Perioperative | The dosage of remifentanil used. |
1 to 10 of 16Source ClinicalTrials.gov
See all 16 registered outcomesOutcomes0
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/NCT07584902
GET https://conductscience.org/api/trials/v1/NCT07584902/registered