The clinical efficiency and safety of laparoscopic hiatal hernia repair with different types of mesh: a prospective randomized multicentre study

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000041410

Enrollment

Unknown

Registered

2020-12-25

Start date

2021-02-01

Completion date

Unknown

Last updated

2021-03-15

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

Conditions

hiatal hernia

Interventions

Experimental group:biological mesh

control group:Synthetic mesh

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients with hiatal hernia during the procedure of laparoscopic hiatal hernia repair at Chaoyang Hospital.

Exclusion criteria

Exclusion criteria: Patients with relapse of esophageal fissures; patients with severe cardiopulmonary and liver and kidney insufficiency; patients with malignant tumors; subjects whose judgmental ability is abnormal or mentally ill.

Design outcomes

Primary

Measure	Time frame
gastroscope;Upper Gastrointestinal Contrast;high resolution manometry,;24 Hour Esophageal pH-Impedance;subjective symptoms;	—

Countries

China

Contacts

Public ContactYang Hui-QI

Beijing Chao-Yang Hospital, Capital Medical University

yang.huiqi@qq.com+86 18301659023

Outcome results

None listed

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