Adding Different Doses of Dexmedetomidine to Bupivecaine in Erector Spinae Plane Block
NCT07923175, Not applicable, Not yet recruiting, Mohamed Mahmoud Soliman
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Adding Different Doses of Dexmedetomidine to Bupivecaine in Erector Spinae Plane Block | ClinicalTrials.gov |
| NCT number | NCT07923175 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 90 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Mohamed Mahmoud Soliman | ClinicalTrials.gov |
| Conditions | Postoperative Pain in Lumbar Spine Surgery | ClinicalTrials.gov |
| Interventions | Erector spinae blane block with bupivecaine only, Erector spinae plane block using bupivecaine plus lower dose dexmedetomidine, Erector spinae plane block using bupivecaine plus higher dose of dexmedetomidine | ClinicalTrials.gov |
| First posted | 2026-11-06 | ClinicalTrials.gov |
| Last updated | 2026-11-06 | ClinicalTrials.gov |
Registered outcomes 7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Visual analogue scale | Mean value of visual analogue scale at 1,4, 8,12,16,20 and 24 hr postoperative. | ClinicalTrials.gov | |
| Secondary | Morphine consumption | 24 hours | The total dose of morphine consumption (intraoperative and postoperative) over the first 24 hrs. | ClinicalTrials.gov |
| Secondary | Heart rate | Heart rate (HR) at 1, 4, 8, 12, 16, 20 and 24 hr postoperative. | ClinicalTrials.gov | |
| Secondary | First analgesia requirement | Time of first analgesic requirement (postoperative 1st dose of morphine) within 24 hours | ClinicalTrials.gov | |
| Secondary | Comlications | 24 hours | nausea, vomiting, dizziness, block failure. | ClinicalTrials.gov |
| Secondary | Mean arterial blood pressure | Mean arterial blood pressure at 1, 4, 8, 12, 16, 20 and 24 hr postoperative | ClinicalTrials.gov | |
| Secondary | Oxygen saturation | Oxygen saturation at 1, 4, 8, 12, 16, 20 and 24 hr postoperative | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)