Trial · NCT07902661
Impact of Intraoperative Neurotization on Sensory Recovery of the Nipple and Breast Skin in Patients Undergoing Nipple Sparing Mastectomy With Immediate Implant-Based Reconstruction: NERSENSE, Prospective Randomized Control Study
NCT07902661, Not applicable, Not yet recruiting, Gangnam Severance Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Impact of Intraoperative Neurotization on Sensory Recovery of the Nipple and Breast Skin in Patients Undergoing Nipple Sparing Mastectomy With Immediate Implant-Based Reconstruction: NERSENSE, Prospective Randomized Control Study. Trials, record NCT07902661. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07902661
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
Impact of Intraoperative Neurotization on Sensory Recovery of the Nipple and Breast Skin in Patients Undergoing Nipple Sparing Mastectomy With Immediate Implant-Based Reconstruction: NERSENSE, Prospective Randomized Control Study
- NCT number
- NCT07902661
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 110 participants, estimated
- Lead sponsor
- Gangnam Severance Hospital
- Conditions
- Breast Cancer
- Interventions
- Nerve anastomosis
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Nipple-Areolar Complex (NAC) Tactile Sensitivity Score | Post-operative Month [예: 6,12,18,24,30,36 months] | Measured using standardized tactile tests (e.g., Semmes-Weinstein monofilaments). |
| Primary | Change in Breast Skin Tactile Sensitivity Score | Post-operative Month [예: 6,12,18,24,30,36 months] | Measured using standardized tactile tests across designated breast skin areas. |
| Secondary | Change in Nipple-Areolar Complex (NAC) Thermal Sensitivity Score | Post-operative Month [예: 6,12,18,24,30,36 months] | Measured using thermal sensitivity testing. |
| Secondary | Change in Breast Skin Thermal Sensitivity Score | Post-operative Month [예: 6,12,18,24,30,36 months] | Measured using thermal sensitivity testing. |
| Secondary | Patient-Reported Outcomes Using Breast-Q Reconstruction Module and 4 Subjective Skin Sensitivity Questions | Post-operative Month [예: 6,12,18,24,30,36 months] | Assessed via the Breast-Q questionnaire and an additional 4-item subjective questionnaire regarding skin sensation. |
| Secondary | Sensory Recovery Comparison According to the Number of Anastomosed Nerve Branches (1, 2, or 3) | Post-operative Month [예: 6,12,18,24,30,36 months] | Comparison of nerve recovery outcomes based on the number of successfully anastomosed nerve branches. |
| Secondary | Post-operative Complications | Post-operative Month [예: 36 months] | Incidence and severity of surgical complications. |
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/NCT07902661
GET https://conductscience.org/api/trials/v1/NCT07902661/registered