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The Clinical Research of Application of the Wireless Analgesia Pump System in Postoperative Analgesia

The Clinical Research of Application of the Wireless Analgesia Pump System in Postoperative Analgesia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054875
Enrollment
Unknown
Registered
2021-12-28
Start date
2021-01-30
Completion date
Unknown
Last updated
2022-12-12

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

Conditions

tumor pain

Interventions

Group 1:Wireless Analgesia Pump System
Group 2:Conventional analgesia

Sponsors

Department of Anesthesiology, National Cancer Center/National Clinical Research Center for Cancer/ Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. ASA I ~ III; 2. Aged 18-70 years, regardless of gender; 3. Voluntarily participate in the study and sign the informed consent form (see Annex 1), without mental disorder and communication barrier, can correctly understand vas scoring rules and use PCIA pump; can cooperate to complete the whole test process. Thoracic surgery, pancreatic and gastric surgery, colorectal surgery, Urology, hepatobiliary and gynecological surgery above grade II shall be selected according to this standard (including open surgery and endoscopic surgery), 4. Postoperative analgesia is needed. A total of 300 patients participated in the clinical trial.

Exclusion criteria

Exclusion criteria: 1. Comatose patients and persons with mental disorders; 2. NSAIDs allergy; 3. History of opioid abuse; 4. Patients with chronic pain and / or long-term use of analgesic drugs or patients who have taken analgesic drugs in recent three months; 5. Unable to cooperate with the study for any reason, such as language understanding, mental illness, etc; 6. Taking other investigational drugs or participating in other clinical trials within 3 months before inclusion in the study; 7. The researchers believe that it is not suitable to be included in this trial.

Design outcomes

Primary

MeasureTime frame
VAS;

Countries

China

Contacts

Public ContactChao Ding

Department of Anesthesiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

13501313926@163.com+86 13501313926

Outcome results

None listed

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