Skip to content

Enhanced Recovery After Surgery in the Application of Laparoscopic Cholecystectomy

Enhanced Recovery After Surgery in the Application of Laparoscopic Cholecystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17010641
Enrollment
Unknown
Registered
2017-02-15
Start date
2017-03-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Cholecystolithiasis

Interventions

A:Take oral glucose solution 2 hours before operation
A:Take oral Tramadol hydrochloride tablets 50mg 2 hours before operation
A:Before the start of surgery with intravenous injection of fluorine noir phenolic ester 50ng.
A:Before the start of surgery with intravenous injection of droperidol 1mg.
A:Postoperative incision infiltration with ropivacaine
A:Began to get out of bed 6 hours after the operation.
A:Begin eating at 6 h after operation.

Sponsors

Medical Center Hospital of Qionglai City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The proposed elective laparoscopic cholecystectomy (LC) in the non acute patients; 2. Aged 18 to 75 years male and female; 3. No contraindication for the surgery and general anesthesia; 4. Cases with independent civil capacity; 5. Color Doppler ultrasound or MRI showed no significant gallbladder effusion; 6. There was no significant thickening of gallbladder wall in CT or MRI, no double loop or multi ring sign; 7. No common bile duct stones or other surgical interventionthe; 8. Patient is willing to accept the treatment; LC; 9. Have no mental illness; 10. Have no obvious hearing or language barriers, the treatment can be a normal exchange; 11. Patients agreed to accept the ERAS treatment; 12. Have not acute or chronic digestive tract obstruction; 13. No delayed gastric emptying.

Exclusion criteria

Exclusion criteria: 1. Does not agree with the implementation of LC; 2. With mental disorders; 3. With definite acute or chronic digestive tract obstruction; 4. With contraindication of LC; 5. With independent civil capacity; 6. Have obvious hearing or language barriers, unable to cooperate; 7. Do not accept ERAS; 8. With history of abdominal operation.

Design outcomes

Primary

MeasureTime frame
Hunger score 2 h before surgery;Pain score 2 h after operation;Abdominal distension score 6 h after operation;6 h postoperative nausea and vomiting score;Pain score 1 d after operation;Hunger score 1 d after surgery;Abdominal distension score 1 d after operation;1 d postoperative nausea and vomiting score;activies of daily living;Postoperative pain control satisfaction;Postoperative nausea and vomiting control satisfactio;Postoperative abdominal distension control satisfactio;Overall satisfaction during hospitalization;Pain score 7 d after operation;7 d postoperative nausea and vomiting score;Abdominal distension score 7 d after operation;Patient satisfaction;

Countries

China

Contacts

Public ContactWu Benhua

Medical Center Hospital of Qionglai City

87239657@qq.com+86 18981838350

Outcome results

None listed

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