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Postoperative analgesia and short- or long-term prognosis of malignancy

Randomized and controlled trials of effect of different postoperative analgesic techniques and drugs on immune function and chronic pain in cancer patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17011092
Enrollment
Unknown
Registered
2017-04-08
Start date
2017-05-02
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

colon/rectal cancer, breast cancer

Interventions

group R:0.2% ropivacaine (PCEA)
group M:morphine (0.5mg/mL, PCIA)
group N:Nalbuphine (1mg/mL, PCIA)
group S:sufentanil (1ug/mL, PCIA)
group F:2mg/mL flurbiprofen axetil combined with 0.8ug/mLsufentanil (PCIA)

Sponsors

Chongqing Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Colorectal cancer patients scheduled undergo elective laparoscopic radical operation or breast cancer patients scheduled undergo elective unilateral modified radical mastectomy will be enrolled. The inclusion criteria: 1) Aged 18 to 75 years; 2) With New York heart association (NYHA)functional class I and II; 3) Biochemical examination CRE<176umol/L.

Exclusion criteria

Exclusion criteria: Patients with any of the following conditions should be excluded in this study 1. History of chronic pain; 2. History of stroke, mental disorder,epilepsy, Parkinson's disease or MMSE11.1mmol/L); (2) Within one month of acute myocardial infarction; (3) With New York heart association (NYHA) functional class above III. 7. Cognitive dysfuntion or unable to communicate accurately; 8. Patients who refused to take part in this study

Design outcomes

Primary

MeasureTime frame
numerical rating scale;Hospital Anxiety and Depression Scale;cortisol;the number of natural killer cell;Th1/Th2 cytokines;incidence of chronic postsurgical pain;adrenocorticotrophic hormone;Confusion Assessment Method for the Intensive Care Unit, CAM-ICU;Incidence of postoperative delirium;

Secondary

MeasureTime frame
ID Pain questionnaire;Ramsay sedation score;mini-mental status examination, MMSE;Richmond Agitation Sedation Scale, RASS;

Countries

China

Contacts

Public ContactLiu Hongliang

Chongqing Cancer Hospital

liuhl75@163.com+86 023-65075687

Outcome results

None listed

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