Impact of using elastic abdominal binder on postoperative pain in women after repeated cesarean section; An open-label randomized control trial

Impact of using elastic abdominal binder on postoperative pain in woman after repeated cesarean section; An open-label randomized control trial

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

TCTR

Registry ID

TCTR20241011001

Enrollment

Registered

2024-10-11

Start date

2024-12-24

Completion date

Unknown

Last updated

2026-03-30

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

Conditions

Postoperative pain after cesarean section between abdominal binder and non-abdominal binder group Elastic abdominal binder, Cesarean section, Previous Caesarean delivery, Postoperative pain, Recovery, Breastfeeding, Wound dehiscence

Interventions

After cesarean section, participant will receive standard of postoperative care in Rajavithi hospital but not offer to use abdominal binder or other similar devices.,After cesarean section, participan

No Intervention No treatment,Experimental Device

Non-abdominal binder group,Abdominal binder group

Eligibility

Sex/Gender

Female

Age

20 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Singleton pregnancy aged 20-45 years, who has low transverse previous cesarean scar, underwent non-emergency cesarean section under spinal anesthesia 2. Understand Thai and can follow instructions

Exclusion criteria

Exclusion criteria: 1. Smoking, alcohol drinking or other substance use 2. Surgery duration exceeding 3 hours 3. Preeclampsia 4. Placenta previa, placenta accreta spectrum 5. Postpartum hemorrhage or needed for blood component transfusion 6. Accidental injury to urinary or gastrointestinal organs 7. Necessary to perform a hysterectomy during cesarean section 8. Postoperative admission to intensive care unit 9. Placement of intraperitoneal drain 10. Circulatory or neuromuscular disease 11. Allergy to abdominal binder 12. Wound complications e.g. infection, hematoma

Design outcomes

Primary

Measure	Time frame
Postoperative pain 24-hour postoperative (apply abdominal binder when patient arrive at postpartum ward) Visual analog score	—

Secondary

Measure	Time frame
Postoperative pain 48-hour postoperative Visual analog score,Postoperative pain 72-hour postoperative Visual analog score,Amout of analgesia use In admission Milligram,Postoperative recovery Postoperative day 2 ObsQoR-10 questionare,Breastfeeding Before discharge LATCH score,Breastfeeding 4-week postoperative Achieve exclusive breastfeeding	—

Countries

Thailand

Contacts

Public ContactPradtana Tangchaisuk

Rajavithi hopital

pradtana.tangchaisuk@gmail.com0880075412

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026