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Effect of Different Analgesic Methods on Postoperative Comfort of Cervical Cancer

Effect of Different Analgesic Methods on Postoperative Comfort of Cervical Cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100041786
Enrollment
Unknown
Registered
2021-01-05
Start date
2021-01-06
Completion date
Unknown
Last updated
2021-03-22

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

Conditions

Cervical Cancer

Interventions

group R:0.5% ropivacaine 30 ml for incision infiltration before closing the abdomen
group I:given PCIA after operation
group E:given PCEA after operation

Sponsors

Taizhou People's Hospital of Jiangsu Province
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients scheduled for elective radical hysterectomy with an ASA physical status I or II, aged 40-65 years, and BMI < 30 kg/m2 were enrolled.

Exclusion criteria

Exclusion criteria: Coagulation disorders, chronic pain, history of allergic reaction to opioids or local anesthetics,severe liver or renal dysfunction, severe hypertension or diabetes.

Design outcomes

Primary

MeasureTime frame
postoperative pain scores;patient satisfaction;

Secondary

MeasureTime frame
complication;

Countries

China

Contacts

Public ContactWen Chuanyun

Taizhou People's Hospital of Jiangsu Province

wen.chuan.yun@163.com+86 18360012198

Outcome results

None listed

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