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Effectiveness of diclofenac plus paracetamol for postoperative pain control after caesarean delivery

Effectiveness of diclofenac plus paracetamol for postoperative pain control after caesarean delivery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20180314003
Enrollment
100
Registered
2018-03-14
Start date
2018-01-17
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

cesarean section under spinal block pain relief cesarean section paracetamol diclofenac

Interventions

placebo 2 tab oral q 8 hr after cesarean section and Patiant controle anesthesia by morphine 1mg/ml,paracetamol(500) 1 tab plus diclofenac(50) 1 tab oral q 8 hr after cesarean section and Patiant cont
Placebo Comparator Drug,Experimental Drug
Placebo,paracetamol(500) plus diclofenac(50)

Sponsors

Udonthani hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: A pregnant woman who have indication for cesarean section under Spinal block

Exclusion criteria

Exclusion criteria: -drug allergy : paracetamol,NSAIDs,OPioids -Underlying disease : Hypertention,Diabetic , heart disease, cerebrovascular disease,Thyroid disease -neuropathy -Increase intracranial pressure or brain lesion -Preeclamsia -Post partum hemorrhage -muscle weakness -All cancer -coagulopathy -acute PID -hemodynamic unstable -Arrythmia -Renal failure -under General anesthesia -Bowel injury -Peptic ulcer perforation

Design outcomes

Primary

MeasureTime frame
Pain releif after cesarean section 24 hour intervention

Secondary

MeasureTime frame
sparing opioids used 24 hour intervention

Countries

Thailand

Contacts

Public Contactsiriluk norsuwan

Udonthani hospital

siriluk.nosuwan@gmail.com+66910567976

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026