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Study on the effect of renal rotation method in the retroperitoneal laparoscopic surgery of massive pheochromocytoma

Study on the effect of renal rotation method in the retroperitoneal laparoscopic surgery of massive pheochromocytoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059953
Enrollment
Unknown
Registered
2022-05-14
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

pheochromocytoma

Interventions

Experimental group:retroperitoneal laparoscopic surgery of massive pheochromocytoma using renal rotation method
Control group with routine retroperitoneal laparoscopic approach:Routine retroperitoneal laparoscopic resection of pheochromocytoma
Control group with routine transabdominal laparoscopic surgery:Routine transabdominal laparoscopic resection of pheochromocytoma

Sponsors

The First Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients aged from 20 to 60; 2. The preoperative diagnosis of pheochromocytoma was clear; 3. Preoperative imaging examination (CT or MRI) showed that the maximum diameter (long diameter) of the tumor was = 10cm; 4. The use of drugs alone cannot keep the blood pressure stable at the normal level; 5. Fully prepared for expansion in accordance with the guidelines before operation (the preparation for expansion shall not be less than 1 month); 6. Agree and sign the informed consent form of the subject.

Exclusion criteria

Exclusion criteria: 1. Patients who cannot take care of themselves; 2. Bilateral or combined with ectopic pheochromocytoma; 3. Previous history of inflammatory infection of the posterior abdominal cavity or surgical operation; 4. Complicated with other serious basic diseases (such as diabetes, arrhythmia, heart failure, low pulmonary function, etc.); 5. Patients with a history of cerebral infarction or myocardial infarction within six months before operation; The preoperative volume expansion is not sufficient and the volume expansion index does not meet the requirements; 6. Change of operation mode during operation or incomplete follow-up data (for the selection of patients in the control group).

Design outcomes

Primary

MeasureTime frame
Blood pressure;Heart rate;BMI index;Hemoglobin;Biochemical indexes of adrenal gland function;Tumor length diameter;Intraoperative bleeding;Operation time;Use of vasoactive drugs during operation (dose and times);Intraoperative blood transfusion;Admission to ICU after operation (duration in ICU);Total postoperative wound drainage;Time length of indwelling wound drainage tube;Pain score;Time point of postoperative ambulation;Total length of hospitalization;

Countries

China

Contacts

Public ContactXiaoming Cao

The First Hospital of Shanxi Medical University

drcxm2@126.com+86 13994205917

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026