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Control,Experiment

2 trials

Sponsors

Siriraj Routine to Research Unit, Faculty of Dentistry, Mahidol University

Conditions

Pregnancy previous cesarean delivery Parecoxib postoperative pain previous cesarean deliveryRoot coverage outcomes of subepithelial connective tissue grafts harvesting from palate before and after recipient site preparation. Viability of palatal subepithelial connective tissue graft harvests. Root coverage outcomes Graft viability Subepithelial connective tissue grafts

Early Phase 1

Root coverage outcomes of subepithelial connective tissue grafts harvesting from palate before and after recipient site preparation and viability of palatal subepithelial connective tissue graft harvests
TCTR20230826008
Faculty of Dentistry, Mahidol UniversityRoot coverage outcomes of subepithelial connective tissue grafts harvesting from palate before and after recipient site preparation. Viability of palatal subepithelial connective tissue graft harvests. Root coverage outcomes Graft viability Subepithelial connective tissue grafts
Start: 2023-06-01Target: 40Updated: 2026-08-03

Unknown Phase

Efficacy of a single intravenous venous dose of Parecoxib 40 mg for post-operative pain control after elective cesarean delivery: a double blind randomized controlled trial
Active, not recruitingTCTR20140618001
Siriraj Routine to Research UnitPregnancy previous cesarean delivery Parecoxib postoperative pain previous cesarean delivery
Start: 2014-07-01Updated: 2026-08-03