buccal acupuncture for pain relief after posterior lumbar spine surgery– a randomized controlled study
Phase 1
- Conditions
- Posterior lumbar spine surgery
- Registration Number
- ITMCTR2200005675
- Lead Sponsor
- ??????????
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
1).ASA grade ?-?
2).Age:40-70years old
3).Willing to accept experimental study treatment and sign informed consent
4).BMI:18.5 kg/m2 -- 23.9 kg/m2
Exclusion Criteria
1). History of fainting needles
2). Puncture site infection
3). Poor compliance
4). Subjects who refused to participate
5). Pregnant or lactating women
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effective pressing times of analgesic pump within 48 hours after operation;visual analogue scale;Sufentanil requirements within 48 hours after surgery;
- Secondary Outcome Measures
Name Time Method Postoperative opioid adverse reactions;Intraoperative remifentanil requirements;