Acute Cholecystitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients who meet the diagnostic criteria of TG13 grade II for acute cholecystitis; 2. Aged between 20 to 69 years old; 3. No gender limitation; 4. No serious internal medicine disease.;Inclusion criteria: 1. Patients who meet the diagnostic criteria of TG13 grade II for acute cholecystitis; 2. Aged between 20 to 69 years old; 3. No gender limitation; 4. No serious internal medicine disease.;Inclusion criteria: 1. Patients who meet the diagnostic criteria of TG13 grade II for acute cholecystitis; 2. Aged between 20 to 69 years old; 3. No gender limitation; 4. No serious internal medicine disease.;Inclusion criteria: 1. Patients who meet the diagnostic criteria of TG13 grade II for acute cholecystitis; 2. Aged between 20 to 69 years old; 3. No gender limitation; 4. No serious internal medicine disease.;Inclusion criteria: 1. Patients who meet the diagnostic criteria of TG13 grade II for acute cholecystitis; 2. Aged between 20 to 69 years old; 3. No gender limitation; 4. No serious internal medicine disease.
Exclusion criteria
Exclusion criteria: 1. combined significantly high risk of anesthesia (ASA IV or above); 2. Combination of serious internal medicine disease and with poor drug control; 3. Have a history of upper abdominal surgery; 4. Do not agree to participate in the study.;Exclusion criteria: 1. combined significantly high risk of anesthesia (ASA IV or above); 2. Combination of serious internal medicine disease and with poor drug control; 3. Have a history of upper abdominal surgery; 4. Do not agree to participate in the study.;Exclusion criteria: 1. combined significantly high risk of anesthesia (ASA IV or above); 2. Combination of serious internal medicine disease and with poor drug control; 3. Have a history of upper abdominal surgery; 4. Do not agree to participate in the study.;Exclusion criteria: 1. combined significantly high risk of anesthesia (ASA IV or above); 2. Combination of serious internal medicine disease and with poor drug control; 3. Have a history of upper abdominal surgery; 4. Do not agree to participate in the study.;Exclusion criteria: 1. combined significantly high risk of anesthesia (ASA IV or above); 2. Combination of serious internal medicine disease and with poor drug control; 3. Have a history of upper abdominal surgery; 4. Do not agree to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| operation time;hospital stays;Total hospitalization expenses; | — |
Secondary
| Measure | Time frame |
|---|---|
| Intraoperative blood loss;conversion rate to the open procedure; | — |
Countries
China
Contacts
The Seventh Affiliated Hospital, Sun Yat-sen university;The Seventh Affiliated Hospital, Sun Yat-sen university;The Seventh Affiliated Hospital, Sun Yat-sen university;The Seventh Affiliated Hospital, Sun Yat-sen university;The Seventh Affiliated Hospital, Sun Yat-sen university