Unknown PHASE4 INTERVENTIONAL NCT00480142

Controlled Release of Oxycodone 10 mg In Pre-Medication For The Post Operative Analgesia In Elective Laparoscopic Bilateral Inguinal Hernia And Elective Laparoscopic Cholecystectomy

Controlled Release of Oxycodone 10 mg In Pre-Medication For The Post Operative Analgesia In Elective Laparoscopic Bilateral Inguinal Hernia And Elective Laparoscopic Cholecystectomy : Prospective Double Blind, Randomized, Placebo-Controlled Study

Sponsor: Kaplan Medical Center

Conditions Elective Laproscopic Bilateral Inguinal Hernia Elective Laproscopic Cholecystectomy

Interventions Oxycodone 10 mg

Updated 5 times since 2017 Last updated: Jun 5, 2007 Started: Jul 31, 2007 Completion: Jul 31, 2008

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

A PHASE4 clinical study on Elective Laproscopic Bilateral Inguinal Hernia and Elective Laproscopic Cholecystectomy, this trial is ongoing. The trial is conducted by Kaplan Medical Center and has accumulated 5 data snapshots since 2007. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

Change History

5 versions recorded

Sep 2024 — Present [monthly]

Unknown PHASE4
Jul 2024 — Sep 2024 [monthly]

Unknown PHASE4

Status: Unknown Status → Unknown
Jan 2021 — Jul 2024 [monthly]

Unknown Status PHASE4
Jun 2018 — Jan 2021 [monthly]

Unknown Status PHASE4
Jan 2017 — Jun 2018 [monthly]

Unknown Status PHASE4

First recorded

Jul 2007

Trial started

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

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Kaplan Medical Center

Data source: Kaplan Medical Center

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

Study Locations

No location information available.