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To evaluate the safety and efficacy of laparoscopic splenectomy assisted by laparoscopy

To evaluate the safety and efficacy of laparoscopic splenectomy assisted by laparoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080672
Enrollment
Unknown
Registered
2024-02-04
Start date
2024-02-15
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

Disease requiring splenectomy

Interventions

Sponsors

Lanzhou University Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) 18 years old =75 years old, gender is not limited (2) The investigator determined that splenectomy was necessary; (3) Able to cooperate with and complete follow-up and related examinations: (4) Voluntarily participate in the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Pregnant or lactating women; (2) Combined with surgical site or systemic infection, severe inflammation; (3) Severe coagulation dysfunction, obvious bleeding tendency (platelets < 50x109 /L); (4) History of major abdominal surgery, intraperitoneal adhesion difficult to separate exposed lesions; (5) have serious comorbidities that cannot tolerate surgery or anesthesia; (6) The lesions directly or directly invade the major blood vessels and invade the surrounding organs; (7) Multiple organ resection (additional surgical removal of surrounding organs); (8) Participants in other investigational drug or device clinical trials have not been completed; (9) Patients considered unsuitable for participation in this project by the investigator.

Design outcomes

Primary

MeasureTime frame
No conversion rate: no conversion from endoscopic system to other endoscopic system, laparoscopic surgery, or open surgery;

Secondary

MeasureTime frame
Operation time;Display effect evaluation;Postoperative pain score;Postoperative hospital stay;

Countries

China

Contacts

Public ContactChen Hao

Lanzhou University Second Hospital

chenhao3996913@163.com+86 150 0946 7790

Outcome results

None listed

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