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Analysis of the Therapeutic Effect of Single-port laparoscopic Inguinal Hernia repair

Analysis of the Therapeutic Effect of Single-port laparoscopic Inguinal Hernia repair

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121425
Enrollment
Unknown
Registered
2026-03-31
Start date
2026-03-31
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Inguinal hernia

Interventions

three incision laparoscopic surgery group:Perform three incision laparoscopic inguinal hernia repair surgery
single-port laparoscopic surgery group:Perform single-port laparoscopic inguinal hernia repair surgery

Sponsors

Shanghai East Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1) Patients with inguinal hernia who are scheduled for laparoscopic surgery. 2) ASA grades I to III. 3) Voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Contraindications for laparoscopic surgery: Patients whose general condition cannot tolerate general anesthesia or laparoscopic surgery. 2) Patients undergoing emergency surgery for incarcerated hernias, strangulated hernias, etc. 3) Patients with severe systemic diseases: such as coagulation dysfunction, decompensated liver cirrhosis, heart failure, severe renal insufficiency, etc. 4) Has participated in other clinical trial studies.

Design outcomes

Primary

MeasureTime frame
SF-36 Quality of Life Score;—

Secondary

MeasureTime frame
Visual Analogue Scale pain score;blood routine examination;Inflammatory markers;Incision satisfaction;—

Countries

China

Contacts

Public ContactTang Rui

Shanghai East Hospital

keintown@126.com+86 189 1876 3707

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026