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Construction and validation of pain prediction model for patients undergoing digestive endoscopy submucosal dissection

Construction and validation of pain prediction model for patients undergoing digestive endoscopy submucosal dissection

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300072854
Enrollment
Unknown
Registered
2023-06-27
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative pain of digestive endoscopic submucosal dissection and its derivative techniques

Interventions

Case series:none

Sponsors

The Anesthesiology Department of Liaocheng People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: ? Age =40 years old; ? Patients undergoing ESD, ESE, EFR, STER and other operations in esophagus, stomach, and intestine; ? Patients with ASA grade I to III.

Exclusion criteria

Exclusion criteria: ? Patients with postoperative routine pump analgesic drugs; ? Patients taking analgesic drugs for non-surgical site pain; ? Patients taking analgesic drugs before surgery; ? Patients with serious postoperative complications (perforation, bleeding, transfer to ICU within 24h after surgery, etc.)

Design outcomes

Primary

MeasureTime frame
Number of analgesic drug applications;Analgesic drug use or not;Time of first use of analgesic drugs after surgery;—

Countries

China

Contacts

Public ContactZongwang Zhang

Liaocheng People's Hospital

zwzhang68@sina.com+86 133 4625 6809

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026