Completed PHASE4 INTERVENTIONAL 2-arm NCT01907984

Diclofenac Administered Before Skull Operations Reduces the Severity of Headache After the Intervention

Preoperatively Administered Single Dose Diclofenac Reduces the Intensity of Acute Postcraniotomy Headache and Decreases Postoperative Analgesic Requirements- a Randomized, Controlled Trial

Sponsor: University of Debrecen

Conditions Intraoperative Analgesic Use Postcraniotomy Headache Postoperative Analgesic Use Postoperative Complications

Interventions Diclofenac Midazolam

Updated 5 times since 2017 Last updated: Jul 22, 2013 Started: Dec 31, 2012 Primary completion: Apr 30, 2013 Completion: Apr 30, 2013

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

Listed as NCT01907984, this PHASE4 trial focuses on Intraoperative Analgesic Use and Postcraniotomy Headache and remains completed. Sponsored by University of Debrecen, it has been updated 5 times since 2012, reflecting limited change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.

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

Dec 2012

Trial started

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

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

University of Debrecen

Data source: University of Debrecen

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

Study Locations

• Debrecen, Hungary