Completed NA INTERVENTIONAL 2-arm NCT02440399

To Compare the Efficacy and Patients' Satisfaction for the Treatment of Post Cesarean Pain of Two Protocols: Oral Medications in Fixed Time Interval Administration Versus Spinal Morphine

Sponsor: HaEmek Medical Center, Israel

Conditions Post Cesarean Pain Management

Interventions Diclofenac Morphine Paracetamol TAB. Percocet (Oxycodone 5MG/Paracetamol 325 MG) Tramadol hydrochloride

Updated 6 times since 2017 Last updated: May 8, 2017 Started: Jul 31, 2015 Primary completion: May 31, 2017 Completion: May 31, 2017

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

A NA clinical study on Post Cesarean Pain Management, this trial is completed. The trial is conducted by HaEmek Medical Center, Israel and has accumulated 6 data snapshots since 2015. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

Change History

6 versions recorded

Sep 2024 — Present [monthly]

Completed NA
Jul 2024 — Sep 2024 [monthly]

Completed NA
Jan 2021 — Jul 2024 [monthly]

Completed NA
Jun 2018 — Jan 2021 [monthly]

Completed NA
Jun 2017 — Jun 2018 [monthly]

Completed NA

Status: Recruiting → Completed

▶ Show 1 earlier version

Jan 2017 — Jun 2017 [monthly]

Recruiting NA

First recorded

Jul 2015

Trial started

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

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

HaEmek Medical Center, Israel

Data source: HaEmek Medical Center, Israel

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

Study Locations

• Afula, Israel