Trial · NCT05270434
Optimal Timing of Endoscopic Intervention in the Treatment of Chronic Pancreatitis.
NCT05270434, Not applicable, Completed, Changhai Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Optimal Timing of Endoscopic Intervention in the Treatment of Chronic Pancreatitis. Trials, record NCT05270434. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05270434
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Optimal Timing of Endoscopic Intervention in the Treatment of Chronic Pancreatitis.
- NCT number
- NCT05270434
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 220 participants, actual
- Lead sponsor
- Changhai Hospital
- Conditions
- Pancreatitis, Chronic
- Interventions
- time interval between ESWL and ERCP is 12h, time interval between ESWL and ERCP is greater than 12h, morphine, buprenorphine, pethidine, tramaldol, metamizole and acetylsalicylacid (Analgesics)
- First posted
- 2022-03-08
- Last updated
- 2025-11-19
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Successful MPD Cannulation Rates | during ERCP procedure | technical success rate of pancreatic cannulation |
| Secondary | Successful clearance of MPD stones | during ERCP procedure | Ductal clearance has been defined as complete, partial, or unsuccessful if the proportion of stones cleared was \> 90 %, 50 %-90 %, or \< 50 %, respectively. |
| Secondary | post-ERCP complications | 30 days | Major post-ERCP complications includes post-ERCP pancreatitis, bleeding, infection, and perforation, which are classified as mild, moderate, or severe, depending mainly on the length of hospitalization and the need for invasive treatment. |
| Secondary | severity of post-ERCP complications | 30 days | severity are classified as mild, moderate, or severe, depending mainly on the length of hospitalization and the need for invasive treatment. |
| Other | Treatment-related costs in RMB from initial enrollment to the end of the study | through endotherapy completion, an average of 14days | The total costs in RMB of each hospitalization |
| Other | The hospitalization time | through endotherapy completion, an average of 14days | Length of hospitalization due to ESWL /ERCP and complications |
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.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 33939679 | BACKGROUND |
Source PubMed
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/NCT05270434
GET https://conductscience.org/api/trials/v1/NCT05270434/registered