RecruitingACTRN12612000706875

Subcutaneous longitudinal acupuncture: a novel and effective approach to acute pain relief in inpatients with rib fracture

Does Subcutaneous longitudinal acupuncture relieve acute pain in inpatients with rib fracture?


Sponsor

Hsin-Yi Ho

Enrollment

60 participants

Start Date

Jan 6, 2012

Study Type

Interventional

Conditions

Summary

Backgorund Pain control is emphasized as a priority for practitioners and patients with rib fracture. Main acute pain management includes analgesia and nerve block. There are some side effects recorded and the effect can’t be continued. All clinical practitioners expect to create a new and safe therapy which could offer long-term pain relief. Acupuncture has been applied to relieve pain for a long time. No clinical trial has taken acupuncture to treat patients with rib fracture currently. Methods and Evaluation This is a prospective, randomized, and single-blind study. A creative therapy named “Subcutaneous longitudinal acupuncture” is applied. Intradermal needle is taken as a control to exclude placebo effect. Evaluation including pain intensity of deep breath, cough, turn over the body, and the angle and rate of turn over the body will be taken before and after needling. Quality of sleep and sustained maximal inspiration (SMI) lung volumes are also recorded. Expected outcome Based on the use of single oral analgesia, the involvement of long needle retention duration of “Subcutaneous longitudinal acupuncture” may relieve acute pain in patients with multiple rib fracture immediately. It may reduce pain when taking deep breath, coughing, and turning over the body, improve sleep quality and recovery of lung function, and decrease the incidence of other lung complications.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This study tests a new type of acupuncture called "subcutaneous longitudinal acupuncture" for people with broken ribs. Rib fractures are very painful, and current treatments have limitations. This technique uses a long needle placed just under the skin along the painful area and left in place. Researchers believe it could provide longer-lasting pain relief compared to standard pain medications alone. You may be eligible if: - You are 18 years or older - You are admitted to the hospital with rib fracture pain - Your pain level is above 5 out of 10 on a pain scale - You are taking ibuprofen 4 times a day - You can clearly describe where your pain is and rate it You may NOT be eligible if: - You cannot breathe deeply, cough, or turn over in bed - You have open wounds on your chest - You have pneumonia, tuberculosis, a serious infection, or a bleeding disorder - You are pregnant Talk to your doctor about whether this trial might be right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

The intervention is subcutaneous longitudinal acupuncture. We used 2.5cm filiform needles to treat the patients. First, we asked the patient to point at the most painful site. We took this most painfu

The intervention is subcutaneous longitudinal acupuncture. We used 2.5cm filiform needles to treat the patients. First, we asked the patient to point at the most painful site. We took this most painful point as an origin of the Y-axis which was parallel with the central line of trunk through the navel. Then we took the transverse line through the navel as the X-axis. The intersection of these two lines was the point which we inserted the needle. After we inserted one needle, we asked the patient to find the most painful site and pointed at it. The same procedure was practiced repeatedly until 5 needles were inserted and taped. In each treatment we used 5 needles totally. The time of retaining needle was 6 hours a day. We treated the patients daily and the overall duration of the treatment was 3 to 5 days based on when the inpatient was discharged from hospital.


Locations(1)

Taoyuan, Taiwan, Province Of China

View Full Details on ANZCTR

For the most up-to-date information, visit the official listing.

Visit

ACTRN12612000706875


Related Trials