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buccal acupuncture for pain relief after posterior lumbar spine surgery– a randomized controlled study

buccal acupuncture for pain relief after posterior lumbar spine surgery– a randomized controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005675
Enrollment
Unknown
Registered
2022-03-03
Start date
2022-02-22
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Posterior lumbar spine surgery

Interventions

Buccal needle group:buccal acupuncture therapy
control group:Nil

Sponsors

??????????
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Effective pressing times of analgesic pump within 48 hours after operation;visual analogue scale;Sufentanil requirements within 48 hours after surgery;—

Secondary

MeasureTime frame
Postoperative opioid adverse reactions;Intraoperative remifentanil requirements;—

Countries

China

Contacts

Public ContactNing Li
1570006368@qq.com15836188308

Outcome results

None listed

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