Recent Updates
Recently added Catalysts

Etoricoxib

Phase 4

Hysterectomy | Small molecule | Pain |Merck & Company, Inc.|Trials Updated: Feb 10, 2017

Etoricoxib development status

Highest phase Phase 4 (NCT00792376)
Phase scored for MRKPhase 3
Registered trials 21 across 8 sponsors since Sep 2004

Success Probability

Subscribe to view

Market & Valuation

Subscribe to view

Trial Design

RandomizedDouble-BlindUNCONTROLLED
Total Trials2
Total Enrollment191

FDA Designations

No designations recorded

Etoricoxib clinical trials

Etoricoxib · 2 trials · 5 indications

Phase 3 1Phase 2 1
NCT00373464Etoricoxib for Routine Post-operative Pain Prophylaxis in Laparoscopic SurgeryHysterectomy
COMPLETED126 Analytics
PHASE3COMPLETED
Etoricoxib for Routine Post-operative Pain Prophylaxis in Laparoscopic Surgery
HysterectomyUnlock trial analytics

Study Endpoints

Primary Endpoints

Equal opioid consumption in both groups postoperatively
Postoperative pain
Within first 5 days after operation
Functional recovery postoperatively
Within first 5 days after operation

Secondary Endpoints

Equal visual analogue scale (VAS) and verbal rating scale (VRS) in the first 4 hours
Unlock Study Endpoints

Study Design & Arms

AllocationRANDOMIZED
MaskingDOUBLE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
ControlPLACEBO_COMPARATORGiven placebo tablets preoperatively
EtoricoxibACTIVE_COMPARATORGiven etoricoxib preoperatively

Interventions

NameTypeDescription
etoricoxibDRUG -
ControlDRUGGiven placebo
Unlock Study Design Details

Eligibility Criteria

Age Range18 Years to 70 Years
SexFEMALE
Healthy VolunteersNo
Study Sites1

Inclusion Criteria: * Patients (American Society of Anaesthesiologists \[ASA\] I and II) due for elective, laparoscopic gynaecologic surgery with the expected need for post-operative opioids: hysterectomy, removal of tube(s) and/or ovarium. * Written informed consent. * Weight between 50 and 120 kg...

Countries:NorwaySingapore
Unlock Eligibility Criteria