Trial · NCT07878013
Intertransverse Process Block Versus Erector Spinae Plane Block for Pain Relief in Lumbar Spine Surgery
NCT07878013, Not applicable, Completed, Hanoi Medical University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Intertransverse Process Block Versus Erector Spinae Plane Block for Pain Relief in Lumbar Spine Surgery. Trials, record NCT07878013. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07878013
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Intertransverse Process Block Versus Erector Spinae Plane Block for Pain Relief in Lumbar Spine Surgery
- NCT number
- NCT07878013
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 90 participants, actual
- Lead sponsor
- Hanoi Medical University
- Conditions
- Postoperative Pain Control, Lumbar Spine Surgery, Degenerative Lumbar Spine Diseases
- Interventions
- Erector Spinae Plane Block, Intertransverse Process Block, Local anesthetic infiltration, Morphine PCA
- First posted
- 2026-10-16
- Last updated
- 2026-10-16
Source ClinicalTrials.gov
Registered outcomes12
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Cumulative Morphine Consumption Within 24 Hours After Surgery | From Hour 0 (awake in the recovery room) to Hour 24 after surgery | Total amount of intravenous morphine (mg) delivered by the patient-controlled analgesia (PCA) pump, including any supplemental morphine, from Hour 0 to Hour 24. Hour 0 is defined as the time the participant is awake in the recovery room and able to self-report pain and use the PCA device. |
| Secondary | Cumulative Morphine Consumption Within 12 Hours After Surgery | From Hour 0 (awake in the recovery room) to Hour 12 after surgery | Total amount of intravenous morphine (mg) delivered by the PCA pump, including any supplemental morphine, from Hour 0 to Hour 12. |
| Secondary | Pain Score at Rest | Hour 0 (awake in the recovery room), and Hours 1, 2, 4, 8, 12 and 24 after surgery | Pain intensity at rest measured on a 0-10 Visual Analogue Scale (0 = no pain, 10 = worst imaginable pain). One score is recorded at each time point. |
| Secondary | Pain Score on Movement | Hour 0 (awake in the recovery room), and Hours 1, 2, 4, 8, 12 and 24 after surgery | Pain intensity on movement measured on a 0-10 Visual Analogue Scale (0 = no pain, 10 = worst imaginable pain). At each time point, the participant is asked to cough and flex the knees, then rates the worst pain experienced during these movements as a single score. |
| Secondary | Total Intraoperative Fentanyl Consumption | From induction of anesthesia to the end of surgery | Total fentanyl dose (µg) from induction of anesthesia to the end of surgery, including the induction dose and supplemental doses given when the PRST score (blood pressure, heart rate, sweating, tearing) is 4 or higher. |
| Secondary | Intraoperative Heart Rate | Before induction, before intubation, after intubation, before skin incision, 5, 15, 30 and 60 minutes after skin incision, before skin closure, and 5 minutes after skin closure. | Heart rate (beats/min) |
| Secondary | Intraoperative Mean Arterial Pressure | Before induction, before intubation, after intubation, before skin incision, 5, 15, 30 and 60 minutes after skin incision, before skin closure, and 5 minutes after skin closure | Mean arterial pressure (mmHg) |
| Secondary | Postoperative Heart Rate | Hour 0 (awake in the recovery room), and Hours 1, 2, 4, 8, 12 and 24 after surgery | Heart rate (beats/min) |
| Secondary | Postoperative Mean Arterial Pressure | Hour 0 (awake in the recovery room), and Hours 1, 2, 4, 8, 12 and 24 after surgery | Mean arterial pressure (mmHg) |
| Secondary | Postoperative Respiratory Rate | Hour 0 (awake in the recovery room), and Hours 1, 2, 4, 8, 12 and 24 after surgery | Respiratory rate (breaths/min) |
1 to 10 of 12Source ClinicalTrials.gov
See all 12 registered outcomesOutcomes0
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.
Papers5
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/NCT07878013
GET https://conductscience.org/api/trials/v1/NCT07878013/registered