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A study of Mallory-Weiss syndrome during gastrointestinal endoscopy

A study of Mallory-Weiss syndrome during gastrointestinal endoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034171
Enrollment
Unknown
Registered
2020-06-27
Start date
2020-08-01
Completion date
Unknown
Last updated
2020-06-29

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

Conditions

Mallory-Weiss syndrome

Interventions

Experimental group:regular air exhausting
Control Group:air exhausting based previous custom

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients with precancerous lesions or early esophageal cancer; 2. Patients who underwent endoscopic mucosal dissection.

Exclusion criteria

Exclusion criteria: Patients who are not eligible for ESD.

Design outcomes

Primary

MeasureTime frame
the rate of Mallory-Weiss syndrome;—

Secondary

MeasureTime frame
the rate of bleeding;the rate of perforation;abdominal pain;bloating;—

Countries

China

Contacts

Public ContactBing Hu

Department of Gastroenterology, West China hospital, Sichuan University

hubingnj@163.com+86 18980601278

Outcome results

None listed

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