Effect of Acupressure on Recovery of Bowel Function in Patients Post Cesarean Section
NCT ID: NCT04620850
Last Updated: 2021-09-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
48 participants
INTERVENTIONAL
2020-11-15
2021-07-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
; Acupressure at ST-36 Zusanli (lateral to anterior crest of tibia, in the tibialis anterior muscle)
Research hypothesis Patients who received acupressure will have earlier flatus passage
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effects of Intraoperative Stimulation of Acupoints on Postoperative Gastrointestinal Motility Recovery
NCT03724656
Effect of Acupressure in The Management of Postmenopausal Constipation
NCT06720077
The Effectiveness of Acupressure on Reducing Pain and Improving Gastrointestinal Function After Laparoscopic Surgery
NCT05360173
The Applying of Acupressure and Abdominal Massage to Improving Constipation in Stroke Patients.
NCT03046563
Abdominal Acupuncture for Gastrointestinal Function Recovery After Gynecologic Laparoscopic Surgery
NCT07293026
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Acupressure
Acupressure after cesarean section 3 hr and then next 3 hr (duration 10 min per time) Acupressure at below knee the point ai locate about4 finger spcae below patella on the lateral side of tibia bone
Acupressure
Acupressure after cesarean section 3 hr and then next 3 hr (duration 10 min per time)
No acupressure
Standard post-operative care
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Acupressure
Acupressure after cesarean section 3 hr and then next 3 hr (duration 10 min per time)
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. General anesthesia
3. Co-operate in research
4. Can speak in thai language
Exclusion Criteria
2. Placenta previa
3. Placental abruption
4. Chorioamnionitis
5. Complication intraoperation (Bowel or bladder injury)
6. Post partum hemorrhage
7. Abdominal adhesion
8. Opertative time more than 2 hour
9. History gastrointestinal surgery
10. Prior acupressure
11. Neurological disease
12. Neuromuscular disease
13. Hepatic disease
18 Years
45 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Department of Medical Services Ministry of Public Health of Thailand
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Sasiwimol kunnitikorn, MD
Role: STUDY_CHAIR
Department of Medical Services Ministry of Public Health of Thailand
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Rajavithi Hospital
Bangkok, , Thailand
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
165/2563
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.