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Curcumin Efficacy for Post-operative Acute Pain in Children Study

Efektivitas penggunaan patch kurkumin dalam mengatasi nyeri orofasial akut pasca tindakan operasi celah bibir dan atau celah langit-langit (In Bahasa) - THE CURCUMIN EFFICACY STUDY

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000053305
Enrollment
75
Registered
2024-01-10
Start date
2020-09-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

This trial was conducted on children with cleft lip and palate that went through a corrective operation for the condition. Once the children went through the operation, all patients received standardised post-operative analgesic drugs. Additionally, patients in the intervention group received curcumin patch placed on their chest. Pain evaluation was performed immediately after the anaesthesia effect wore off, and eight hours after the placement of the curcumin patch. Pain evaluation was performe

Interventions

The control group. Patients only received standard post-surgery drug. First intervention group. Patients received standard post-surgery drug + curcumin patch that contains piperine Second intervention

Sponsors

Faculty of Dentistry, University of Padjadjaran
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Aged 36 months old or less; - Had an initial pain score of (a minimum of) 1 (according to the FLACC pain score); - Not allergic to curcumin and or piperine and - Did not have any injuries or inflammation at other areas of the body that might act as another source of pain. - Willing to participate

Exclusion criteria

Exclusion criteria: Participants were excluded from the study if: - participants consumed another analgesic agent aside from the ones prescribed or - participants removed the patch (those who were assigned to the treatment groups) before eight hours of application,

Design outcomes

Primary

MeasureTime frame
The decrease of pain level through PGE2 saliva level measurement

Secondary

MeasureTime frame
The decrease of pain level through Face, Leg, Activity, Cry and Consolability (FLACC) scale scoring

Countries

Asia(except Japan)

Contacts

Public ContactTantry Maulina

University of Padjadjaran, Bandung, Indonesia Oral Surgery Department, Faculty of Dentistry

tantry.maulina@unpad.ac.id62222514985

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026