Trial · NCT02678117
Analgesic Potentials of Preoperative Pregabalin,Magnesium Sulphate and Their Combination in Acute Post-thoracotomy Pain
NCT02678117, Phase 3, Completed, National Cancer Institute, Egypt
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Analgesic Potentials of Preoperative Pregabalin,Magnesium Sulphate and Their Combination in Acute Post-thoracotomy Pain. Trials, record NCT02678117. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02678117
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Analgesic Potentials of Preoperative Pregabalin,Magnesium Sulphate and Their Combination in Acute Post-thoracotomy Pain
- NCT number
- NCT02678117
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 120 participants, actual
- Lead sponsor
- National Cancer Institute, Egypt
- Conditions
- Postoperative Pain
- Interventions
- Pregabalin & Placebo, Magnesium sulphate & Placebo, Pregabalin & Magnesium sulphate, Placebo
- First posted
- 2016-02-09
- Last updated
- 2021-09-22
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Total morphine consumption | First 24 hours in postoperative period | patients are given regular intravenous morphine through patient controlled analgesia (PCA) and morphine consumption calculated from the PCA device |
| Secondary | Pain intensity using Visual Analogue Scale | First 24 hours in postoperative period | Assessment of pain intensity every 4 hours in the first 24 hours in postoperative period |
| Secondary | Recovery Time | Immediately after ending the surgery | Time taken for recovery of the patient to be fully awake |
| Secondary | Heart Rate | First 24 hours in postoperative period | Assessment of Heart Rate every 4 hours |
| Secondary | Blood Pressure | First 24 hours in postoperative period | Assessment of Blood Pressure every 4 hours |
| Secondary | Oxygen saturation | First 24 hours in postoperative period | Assessment of Oxygen saturation every 4 hours |
| Secondary | Respiratory Rate | First 24 hours in postoperative period | Assessment of Respiratory Rate every 4 hours |
| Secondary | Postoperative nausea and vomiting | First 24 hours in postoperative period | Postoperative nausea and vomiting scale (none 0, mild 1, moderate 2 , sever 3) |
| Secondary | Side effects from the used drugs | First 24 hours in postoperative period | |
| Secondary | Sedation score | First 24 hours in postoperative period | Using Ramsay Sedation score |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers3
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT02678117
GET https://conductscience.org/api/trials/v1/NCT02678117/registered