Explore multiple analgesic regimens of integrated traditional Chinese and western medicine: single-blind, randomized, multicenter, phase II clinical study
- Conditions
- ung cancer, pancreatic cancer, esophageal cancer
- Registration Number
- ITMCTR2000004032
- Lead Sponsor
- Affiliated Hospital of Southwest Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- Not specified
(1) Aged 18 to 70 years old male or female;
(2) the patients were mainly diagnosed as lung cancer, pancreatic cancer and esophageal cancer by histo athological biopsy;
(3) the estimated survival time is more than 3 months;
(4) have tumor-related pain and be able to score cancer pain independently;
(5) the corresponding painkillers have been taken according to the three-step analgesic method, and the cancer pain is basically stable;
(6) the patients and their families can have good communication skills, voluntarily participate in this trial and sign a written informed consent form. Be able to adhere to and follow the requirements of the program.
(1) patients with pain caused by other non-cancerous factors;
(2) patients have severe or uncontrolled systemic diseases or diseases that researchers believe are not suitable for patients to participate in the trial, including skin diseases (such as local skin ulceration of the auricle or those with a history of skin allergy not suitable for auricular point application), severe hypertension, heart disease and so on;
(3) pregnant and lactating women;
(4) it is determined by the researchers that it is not suitable for patients to participate in this trial.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain NRS score;Incidence and remission of adverse reactions during treatment;Quality of life score of tumor patients;The frequency and duration of the outbreak of pain, the relief time of rescue dose and the degree of pain relief.;Changes in oral dose of painkillers;
- Secondary Outcome Measures
Name Time Method