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NCT06360692
Impact of Nipple Micropigmentation in Mastectomized Women
trial in Body Image in 30 participants. Not yet recruiting.
30 October 2024
Quick facts
| Lead sponsor | Cardenal Herrera University |
|---|---|
| Status | Not yet recruiting |
| Study type | OBSERVATIONAL |
| Enrollment | 30 |
| Start date | 1 June 2024 |
| Primary completion | 30 October 2024 |
| Estimated completion | 31 December 2025 |
Conditions studied
- Body Image — all drugs for Body Image →
- Female Sexual Function — all drugs for Female Sexual Function →
- Self Esteem — all drugs for Self Esteem →
- Intimacy With Your Partner — all drugs for Intimacy With Your Partner →
Sponsor
Cardenal Herrera University
Who can join
18 and older, female only, with Body Image or Female Sexual Function. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This will be a multicenter prospective descriptive case series study following a cohort. The micropigmentation/tattoo procedure will be carried out following the protocol established in each center (see annex x). The present investigation only involves measuring the impact that this technique has on the patients by collecting data in digital format before and after the CAP micropigmentation/tattoo that motivated their visit to the clinical service. CAP micropigmentation/tattooing is usually performed between 6 and 12 months after the breast reconstructive surgery has been completed, sufficient time for healing to complete and the breast to stabilize, although it can be performed from 2 months after the intervention. Nurses are responsible for performing micropigmentation/tattooing of the areola and nipple in mastectomized women.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06360692
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06360692 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Cardenal Herrera University
- Last refreshed: 11 April 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06360692.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing