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CompletedNCT06658990Updated Oct 26, 2024

Effect of Ultrasound Positioning Assisted Cheek Needle Therapy on Postoperative Recovery Quality of Patients with Radical Resection of Lung Cancer

An interventional study of buccal acupuncture and control in Surgery, sponsored by Northern Jiangsu People's Hospital. Completed at 1 site in China. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2024-10-26.

Sponsored by Northern Jiangsu People's Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled Feb 2024, registered Oct 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
136
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

To explore the effect of ultrasound positioning assisted buccal acupuncture on postoperative pain and recovery quality of patients undergoing thoracoscopic radical resection

02

Conditions studied

  • Surgery
03

In context

Lead sponsor

Northern Jiangsu People's Hospital is the lead sponsor of 60 studies on the registry; 31 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Tracheal intubation under general anesthesia
  2. Young and middle-aged patients aged 18-65 years
  3. BMI: 18.5-28kg /m2

Exclusion criteria

Exclusion Criteria:

  1. head and facial trauma, infection, disease
  2. more than 2 kinds of coronary heart disease, hypertension, stroke, diabetes, immune disease and other diseases before surgery
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
136 participants (actual)

Study arms

  • Experimental
    buccal acupuncture

    Procedure: buccal acupuncture

  • Active comparator
    control

    Drug: control

Interventions

  • Procedurebuccal acupuncture

    ultrasound positioning assisted buccal acupuncture

  • Drugcontrol

    Sufentanil is used after surgery

06

What researchers measure

Primary outcomes

  1. Number of additional analgesics

    Time frame: 7 days

07

Study locations

1 site
  • Wang Mengyao
    Yangzhou, Jiangsu 225000, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 26, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06658990
Lead sponsor
Northern Jiangsu People's Hospital
Responsible party
Sponsor
First posted
Oct 26, 2024
Start date
Feb 1, 2024
Primary completion
Jun 30, 2024
Completion
Jun 30, 2024
Last update
Oct 26, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2024. You cannot join it, but the record below documents what was studied.

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