Trial · NCT07877740
Feasibility of a Standardized Fascial Plane Block Protocol for Breast Cancer Surgery
NCT07877740, Not yet recruiting, Hôpital Fribourgeois
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Feasibility of a Standardized Fascial Plane Block Protocol for Breast Cancer Surgery. Trials, record NCT07877740. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07877740
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Feasibility of a Standardized Fascial Plane Block Protocol for Breast Cancer Surgery
- NCT number
- NCT07877740
- Status
- Not yet recruiting
- Enrollment
- 65 participants, estimated
- Lead sponsor
- Hôpital Fribourgeois
- Conditions
- Breast Cancer Surgery, Locoregional Anaesthesia, Hypnosis, Fascial Plane Block
- Interventions
- Standardized locoregional anesthesia protocol for breast cancer surgery
- First posted
- 2026-10-16
- Last updated
- 2026-10-16
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Successful completion of surgery without conversion to general anesthesia | Intraoperative period (from surgical incision to end of surgery) | Proportion of participants in whom surgery is completed under locoregional anesthesia without conversion to general anesthesia requiring airway instrumentation. |
| Secondary | Patient acceptance | Preoperative period (before surgery) | Proportion of eligible patients accepting the proposed locoregional anesthesia pathway. |
| Secondary | Adherence to the standardized protocol | Periprocedural | Proportion of enrolled participants in whom the standardized protocol is applied as planned. |
| Secondary | Anesthesia induction time | Periprocedural (before surgical incision) | Time from participant arrival in the operating room to surgical incision. |
| Secondary | Surgeon satisfaction | Intraoperative period (immediately after surgery) | Surgeon satisfaction with operative conditions assessed using a 5-point Likert satisfaction scale, ranging from 1 (very dissatisfied) to 5 (very satisfied), with higher scores indicating greater satisfaction |
| Secondary | Patient satisfaction | Perioperative period (before hospital discharge) | Patient satisfaction with anesthetic management assessed using a 5-point Likert satisfaction scale, ranging from 1 (very dissatisfied) to 5 (very satisfied), with higher scores indicating greater satisfaction. |
| Secondary | Perioperative complications | Perioperative period (from anesthesia start to hospital discharge) | Incidence of complications related to locoregional anesthesia, sedation, hypnosis, or conversion to general anesthesia. |
| Secondary | Reasons for conversion to general anesthesia | Intraoperative period | Description of reasons leading to conversion, when applicable. |
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.
Papers11
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/NCT07877740
GET https://conductscience.org/api/trials/v1/NCT07877740/registered