Trial · NCT07913789
Opioid Free Anesthesia Combined With Pectoral Nerve Block (PECS Block) in Breast Cancer Surgery
NCT07913789, Not applicable, Completed, Tanta University
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Opioid Free Anesthesia Combined With Pectoral Nerve Block (PECS Block) in Breast Cancer Surgery. Trials, record NCT07913789. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07913789
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Opioid Free Anesthesia Combined With Pectoral Nerve Block (PECS Block) in Breast Cancer Surgery
- NCT number
- NCT07913789
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 60 participants, actual
- Lead sponsor
- Tanta University
- Conditions
- Opioid Free Anesthesia, Pectoral Nerve Block, Breast Cancer Surgery
- Interventions
- Opioid Free Anesthesia, Opioid based anesthesia
- First posted
- 2026-11-03
- Last updated
- 2026-11-03
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Total morphine consumption | 24 hours postoperatively | For each patient with \[Visual Analogue Scale (VAS) \> 4\], 3 mg of morphine will be prescribed as rescue analgesia to be repeated after 30 min if pain persists until the VAS\< 4. |
| Secondary | Heart rate | Till the end of surgery (Up to 2 hours) | Heart rate was recorded at baseline, after performing of block, and every 15 min till the end of surgery. |
| Secondary | Mean arterial blood pressure | Till the end of surgery (Up to 2 hours) | Mean arterial blood pressure was recorded at baseline, after performing of block, and every 15 min till the end of surgery. |
| Secondary | Degree of pain | 24 hours postoperatively | All the participants were explained about postoperative pain assessment with the visual analogue scale (VAS), from 0 to 10 (0 represents "no pain" while 10 represents "the worst pain imaginable") |
| Secondary | Time to extubation | Till the extubating (Up to 60 minutes) | The time to extubate was counted starting from stoppage of inhalational anesthetic agent till the extubating was practiced. |
| Secondary | Quality of recovery | 24 hours postoperatively | Quality of recovery was assessed using Modified Aldrete Score (depending on conscious level, activity of the patient, breathing, blood pressure, oxygen saturation). |
| Secondary | Time to the 1st rescue analgesia | 24 hours postoperatively | Time to the first request for the rescue analgesia was recorded from end of surgery to first dose of morphine administrated. |
| Secondary | Incidence of side effects | 24 hours postoperatively | Incidence of side effects such as bradycardia, hypotension, nausea, vomiting, respiratory depression, hematoma at the site of injection, and local anesthetic toxicity were recorded. |
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.
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/NCT07913789
GET https://conductscience.org/api/trials/v1/NCT07913789/registered