A randomized controlled study of local analgesia in the recovery of digestive tract surgery

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IPR-17010452

Enrollment

Unknown

Registered

2017-01-16

Start date

2017-02-03

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

Digestive tract cancer

Interventions

A:Patient-controlled intravenous analgesia

B:Incision / drainage tube local anesthetic infiltration

C:Patient-controlled intravenous analgesia +Incision / drainage tube local anesthetic infiltration

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-80 years male and female; 2. hospitalized patients; 3. digestive tract surgery patients (malignant tumor, stromal tumor); 4. patients undergoing laparoscopic surgery; 5. voluntary participation and informed consent; 6. compliance can be completed assessment.

Exclusion criteria

Exclusion criteria: 1. emergency surgery patients; 2. mentally ill or unable to cooperate; 3. general condition is poor, >ASA III; 4. life expectancy is not more than 24 hours of dying patients; 5. ropivacaine drug allergy and tolerance; 6. drugs or alcohol abusers; 7. pregnant or lactating women.

Design outcomes

Primary

Measure	Time frame
Anal exhaust time;Pain score;	—

Secondary

Measure	Time frame
Quality of Life Score;CRP;TNF-a;IL-6;Corticosteroid hormone;	—

Countries

China

Contacts

Public ContactNiu Zhaojian

Affiliated Hospital of Qingdao University

niuzj@hotmail.com+86 18661808077

Outcome results

None listed

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