Trial · NCT07344467
Oral Melatonin Versus Oral Pregabalin on Postoperative Pain and Anxiety Following Spine Surgery
NCT07344467, Not applicable, Recruiting, Tanta University
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Oral Melatonin Versus Oral Pregabalin on Postoperative Pain and Anxiety Following Spine Surgery. Trials, record NCT07344467. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07344467
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Oral Melatonin Versus Oral Pregabalin on Postoperative Pain and Anxiety Following Spine Surgery
- NCT number
- NCT07344467
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 105 participants, estimated
- Lead sponsor
- Tanta University
- Conditions
- Oral, Melatonin, Pregabalin, Postoperative Pain, Anxiety, Spine Surgery
- Interventions
- Placebo capsule, Melatonin capsule, Pregabalin capsule
- First posted
- 2026-01-15
- Last updated
- 2026-01-21
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Degree of pain | 3 days postoperatively | Postoperative pain will be assessed using the Visual Analogue Scale (VAS) at the following time points: upon arrival to the Post-Anesthesia Care Unit (PACU), and at 1, 2, 4, 6, 8, 12, and 24 hours, as well as at 12 and 24 hours on postoperative days 2 and 3. |
| Secondary | Incidence of postoperative anxiety | 3 days postoperatively | Postoperative anxiety will be assessed using the Hospital Anxiety and Depression Scale (HADS) at the following time points: * 2, 6, and 24 hours on postoperative day 1, * 12 and 24 hours on both postoperative days 2 and 3. According to the HADS scoring system: 1. A score of 0-7 is considered normal, 2. 8-10 indicates a borderline case, 3. 11-21 reflects abnormal anxiety. This assessment timeline enables comprehensive monitoring of anxiety levels during the critical early postoperative period |
| Secondary | Postoperative analgesic consumption | 3 days postoperatively | Postoperative analgesic consumption will be recorded. |
| Secondary | Postoperative sleep quality | 3 days postoperatively | Postoperative sleep quality will be recorded before surgery and every day for three days postoperative. |
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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.
Source
- Release
- trials-2026-11-12-0.4.0
- Release manifest SHA-256
- 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
- Registry capture
- 2026-11-12
- Results copy, AACT
- 2026-03-23
- NIH clinical studies file
- 2026-11-13
Source ClinicalTrials.gov
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone 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/NCT07344467
GET https://conductscience.org/api/trials/v1/NCT07344467/registered