Completed PHASE4 INTERVENTIONAL 2-arm NCT01902108

Added Value of Local Clonidine for Spine Postoperative Pain Control, in Addition to Bupivacaine

Randomized Double-blind Trial Comparing the Post-operative Analgesic Efficacy of Local Wound Infiltration With Bupivacaine Alone to Bupivacaine With Clonidine in Posterior Spine Surgeries

Sponsor: St Joseph University, Beirut, Lebanon

Conditions Post-operative Pain

Interventions Bupivacaine Clonidine

Updated 5 times since 2017 Last updated: Dec 6, 2015 Started: Jan 31, 2013 Primary completion: Dec 31, 2015 Completion: Dec 31, 2015

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

This PHASE4 trial investigates Post-operative Pain and is currently completed. St Joseph University, Beirut, Lebanon leads this study, which shows 5 recorded versions since 2013 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.

Status Flow

Change History

5 versions recorded

Sep 2024 — Present [monthly]

Completed PHASE4
Jul 2024 — Sep 2024 [monthly]

Completed PHASE4
Jan 2021 — Jul 2024 [monthly]

Completed PHASE4
Jun 2018 — Jan 2021 [monthly]

Completed PHASE4
Jan 2017 — Jun 2018 [monthly]

Completed PHASE4

First recorded

Jan 2013

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

St Joseph University, Beirut, Lebanon

Data source: St Joseph University, Beirut, Lebanon

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

• Beirut, Lebanon