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A clinical trial to evaluate the efficacy and safety of laparoscopic herniorrhaphy assisted by laparoscopic system

A clinical trial to evaluate the efficacy and safety of laparoscopic herniorrhaphy assisted by laparoscopic system

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077106
Enrollment
Unknown
Registered
2023-10-31
Start date
2023-10-31
Completion date
Unknown
Last updated
2023-11-06

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

Conditions

Hernia of abdominal wall

Interventions

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1)18 years old = 75 years old, regardless of sex; (2) those who need abdominal hernia repair according to the researcher's judgment; (3) Be able to cooperate and complete the follow-up and related examinations; (4) Voluntary participation in this study and signing of informed consent.

Exclusion criteria

Exclusion criteria: (1) pregnant or lactating women; (2) strangulated hernia; (3) Emergency operations such as necrosis, perforation and obstruction; (4) Combined with surgical site or systemic infection and severe inflammatory reaction; (5) Severe coagulation dysfunction and obvious bleeding tendency (platelets < <100x109/L); (6) Severe complications and inability to tolerate surgery or anesthesia; (7) Those who have not completed the clinical trials of other research drugs or devices; (8) Patients that the researcher thinks are not suitable to participate in this project.

Design outcomes

Primary

MeasureTime frame
Non-conversion rate of operation;

Secondary

MeasureTime frame
Postoperative hospitalization time;Intraoperative blood loss and blood transfusion rate; Operation time;Postoperative pain score;Incidence rate of instrument defects;

Countries

China

Contacts

Public ContactChen jie

Peking University People's Hospital

chenjiejoe@vip.sina.com+86 138 1013 8411

Outcome results

None listed

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