Pain Relief Effect of Angiopuncture for Patients With Postoperative Pain

NCT ID: NCT05938348

Last Updated: 2023-07-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 41 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-01-01
• Study Completion Date: 2022-06-01

Brief Summary

The study aimed to investigate the effectiveness of angiopuncture therapy in pain alleviation for postoperative pain patients. The study involved patients aged 20-65 with acute foot and ankle trauma and pain after surgery. Physicians used handheld ultrasound Doppler to measure perforators, puncture participants with a filiform needle, and monitor pain scores and heart rate data before and after acupuncture. The duration of therapy was 20 minutes per day for 72 hours, with pain measured using the numerical rating scale. The study aimed to compare the outcomes before and after angiopuncture.

Detailed Description

In order to give therapeutic therapy, solid filiform needles are inserted into the skin during dry needling (DN), traditional acupuncture (TA), and western medical acupuncture (WMA). DN is a treatment used to treat painful musculoskeletal illnesses, whereas TA and WMA have a wider variety of indications, including musculoskeletal discomfort, gastrointestinal problems, and neurological concerns. While DN implants are used in trigger points, acupuncture is for acupoints.

In addition, common methods include injections of painkillers, oral medications, and nerve blocks. Angiopuncture therapy is being used for the first time as a method of pain management in this article. The aim was to investigate if skin perforating needling therapy could alleviate postoperative pain in patients.

Patients with recent foot and ankle surgery who have had acute foot and ankle injuries and pain. Doctors measured three to four perforators at the proximal end of the trauma site using a handheld ultrasound Doppler, punctured the perforators for 15 minutes with a filiform needle (size: 0.18mm gauge * 25mm length), and then monitored the patient's pain level and heart rate data before and after acupuncture Variety. If pain relief is possible, they'll do it. Risks include becoming more painful.

To create numbers, investigators employed an internet table generator. Despite having just one group, investigators compared the results of angiopuncture before and after therapy lasts for 20 minutes per day for 72 hours. Numeric rating scale (NRS) pain score at baseline: 6, 12, 24, 36, 48, 60, and 72 hours.

Conditions

Postoperative Pain

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

pain scores of patients before and after (6h, 12h, 24h, 48h, 72h) angiopuncture.

investigators done angiopuncture on perforators in human. Pain score will be assessed on both before and after the treatment.

Group Type: EXPERIMENTAL

angiopuncture

Intervention Type: BEHAVIORAL

we conducted acupuncture on perforators by using acupuncture needles.

Interventions

angiopuncture

we conducted acupuncture on perforators by using acupuncture needles.

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• aged 20-65 years
• acute foot or ankle trauma
• pain after foot or ankle surgery

Exclusion Criteria

• Have scars and deformities on the lower extremity surface
• cannot cooperate with the locating method of angiopuncture
• allergy to any material
• pregnant women
• breastfeeding women

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

City University of Hong Kong

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Gaomi People'S Hospital

Gaomi, Shandong, China

Countries

China

References

Han R, Feng W, Guo C, Ding Z, Hu J. Pain relief effect of angiopuncture therapy on patients with postoperative pain: A clinical trial. Medicine (Baltimore). 2024 Jan 12;103(2):e36847. doi: 10.1097/MD.0000000000036847.

Reference Type: DERIVED

PMID: 38215127 (View on PubMed)

Other Identifiers

111111

Identifier Type: -

Identifier Source: org_study_id