The trial was performed on post-cleft lip and cleft palate paediatric patients.
Conditions
Interventions
Control 1: the group did not receive any intervention. Pain scoring was measured twice. The first one was immediately after the anaesthesia effect worn off. And the second one is eight hours after the
Sponsors
Faculty of Dentistry, University of Padjadjaran.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Inclusion criteria: 1) had completed the cleft lip and/or cleft palate surgery procedure; 2) aged 36-month-old or less; 3) had no allergic history to curcumin; 4) has an initial pain score of 3 or greater than 3 on a scale of 0-10; 5) did not have any injuries at other parts of the body that have the potential to cause pain, aside from the postoperative wounds.
Exclusion criteria
Exclusion criteria: Exclusion criteria: 1) consumed additional pain or anti-inflammatory medication in addition to the curcumin patch or the standard analgesic medication prescribed by the doctor in charge; 2) removed the curcumin patch position from the initial location given by the investigator during the study period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The score of the Face, Leg, Activity, Cry, and Consolability (FLACC) scale as pain indicator. The FLACC scores were measured twice. The basic measurement was immediately after the anaesthesia effect worn off, and the second one is eight hours after the first measurement. | — |
Countries
Asia(except Japan)
Contacts
Public ContactTantry Maulina
Faculty of Dentistry, University of Padjadjaran Oral and Maxillofacial Surgery Department.
Outcome results
None listed