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Cold therapy for pain relief in postoperative cesarean section ; randomized controlled trial

Cold therapy for pain relief in postoperative cesarean section ; randomized controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190605007
Enrollment
Unknown
Registered
2019-06-05
Start date
2018-12-11
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

Cold pack gel complication Surgical site infection

Interventions

Control group received standard routine postoperative care consisted of vital sign recording&#44
intravenous fluid&#44
input/output recording&#44
an analgesic drugs&#44
an antibiotic&#44
foley’s catheter retention and surgical wound dressing with a waterproof transparent patch ,Group number was concealed in sealed envelopes that were opened after completion of the surgery. Surgeons
consisted of vital sign recording&#44
foley’s catheter retention and surgical wound dressing with a waterproof transparent patch (tegadermR with pad or Op&#45
site). Participants in the intervention group received cold pack gel with its own thin fabric bag that was kept at &#45
4°C. Then&#44
cold pack gel was placed on surgical wound dressing at 2 hours after surgery for 6 hours of duration. It was changed every two hours for preserving cold temperature. Control group received standard ro
12 and 24 hours after surgery. Participants were asked to choose a number from 0 (no pain) to 10 (the worst pain) to describe their pain.
No Intervention Other,Experimental Device
Control group,Cold pack group

Sponsors

TU research fund for students
Lead Sponsor
TU research fund for students
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: pregnant women who underwent cesarean section under spinal block with 0.5% heavy marcaine and morphine 0.2 mg (Total 2-2.2ml) , with pfannenstiel incision, age more than 18 years old

Exclusion criteria

Exclusion criteria: underlying disease as cold urticaria and raynuad phenomenon, infection at surgical site, active skin lesion at surgical site

Design outcomes

Primary

MeasureTime frame
postoperative VAS scores in cold pack group compare to control group 2, 6, 12 and 24 hours after surgery VAS scores

Secondary

MeasureTime frame
Pethidine comsumption 24 hours after surgery Pethidine comsumption (mg) within 24 hours after surgery,Time for first dose of pethidine requirement first dose of pethidine requirement Nurse recording,Length of hospital stay since admission until discharge Medical record

Countries

Thailand

Contacts

Public ContactMathavee Chaowalit

Faculty of medicine, Thammasat university

maray.maythavee@gmail.com0971303170

Outcome results

None listed

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