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NCT04917614 Clinical Trial

Effect of Transcutaneous Electrical Acupoint Stimulation on Obstetric Quality of Recovery-10 After Cesarean Section

Recovery Clinical Trial

Official title:
Effect of Transcutaneous Electrical Acupoint Stimulation on Obstetric Quality of Recovery-10 After Cesarean Section

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04917614
Other study ID # TEAS and ObsQoR-10
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 18, 2021
Est. completion date January 24, 2022

Study information
Verified date January 2022
Source Konya Meram State Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary aim of this prospective and randomized trial is to investigate the effect of TEAS on postoperative recovery using the Obstetric Quality of Recovery-10 questionnaire in patients undergoing elective cesarean section.

Description:

Acupoint stimulation is postulated to modulate neurological signal transmission through afferent nociceptive pathways. Acupoint stimulation has been associated with positive effects on perioperative symptoms such as nausea, pain, and sleep disturbance. Transcutaneous electrical acupuncture point stimulation (TEAS) is an acupuncture treatment developed by combining traditional Chinese acupuncture with transcutaneous electrical nerve stimulation. TEAS has proven to be effective in postoperative pain and nausea-vomiting by applying a current of different frequencies, intensities, and waveforms through electrodes adhering to the skin. Using TEAS may relieve perioperative symptoms without increasing the risk of drug-related adverse events and alleviate and improve the patient's health condition, including the postoperative perspective.

Recruitment information / eligibility
Status Completed
Enrollment 86
Est. completion date January 24, 2022
Est. primary completion date January 24, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 48 Years
Eligibility Inclusion Criteria: - Elective cesarean operation - Able to give informed consent Exclusion Criteria: - Patients with neurological or psychological diseases - patients with chronic analgesic and antidepressant drug use - Patients unable to communicate - Patients previously treated with TEAS or acupuncture, - Patients with heart failure and have pace-maker, - patient with local infection in the TEAS area

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Transcutaneous Electrical Acupoint Stimulation
Transcutaneous Electrical Acupoint Stimulation

Locations
Country Name City State
Turkey Betul Kozanhan Konya

Sponsors (1)
Lead Sponsor Collaborator
Konya Meram State Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Quality of Recovery Obstetric Quality of Recovery-10 (ObsQoR-10©) Scoring Tool The first 24 hours postoperatively
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