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Effect of Acupressure on Recovery of Bowel Function in Patients Post Cesarean Section

Effect of Acupressure on Recovery of Bowel Function in Patients Post Cesarean Section

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04620850
Enrollment
48
Registered
2020-11-09
Start date
2020-11-15
Completion date
2021-07-30
Last updated
2021-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acupressure, Bowel Ileus, Cesarean Section, Post-Op Complication

Brief summary

Research objectives To compare the efficacy of acupressure with no acupressure to examine time to first flatus in patient post cesarean section ; 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

Detailed description

Research design Randomized controlled trial. Compare between The investigators is who assess the acupressure with control group is the participants do not assess the acupressure

Interventions

DEVICEAcupressure

Acupressure after cesarean section 3 hr and then next 3 hr (duration 10 min per time)

Sponsors

Department of Medical Services Ministry of Public Health of Thailand
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

1. Pregnancy woman age 18-45 years 2. General anesthesia 3. Co-operate in research 4. Can speak in thai language

Exclusion criteria

1. Twin pregnancy 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

Design outcomes

Primary

MeasureTime frameDescription
To study the duration of the first time to flatus passage in post cesaren section patientthrough study completion, an average of 1 yearthe duration ; hour after post cesaren section

Secondary

MeasureTime frameDescription
To study the duration of the first time to have bowel sound in post cesaren section patientthrough study completion, an average of 1 yearthe duration ; hour after post cesaren section
To study the duration of the first time to pass stool in post cesaren section patientthrough study completion, an average of 1 yearthe duration ; hour after post cesaren section
To study the symptomatic about Nausea/vomiting in post cesaren section patientmildScore; mild,moderate,severe

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026