# Study on the Efficacy and Safety of a Device for Post-op Recovery in Pediatric Adenectomy/Adenotonsillectomy.

> **NCT06478433** · NA · NOT_YET_RECRUITING · sponsor: **Pharmaluce srl** · enrollment: 90 (estimated)

## Conditions studied

- Adenoidal Disorder
- Tonsillitis
- Otorhinolaryngologic Diseases
- Nasal Disease

## Interventions

- **DEVICE:** Munatoril Aerosol Combo
- **DEVICE:** Iperclenny

## Key facts

- **NCT ID:** NCT06478433
- **Lead sponsor:** Pharmaluce srl
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** NOT_YET_RECRUITING
- **Start date:** 2024-12-01
- **Primary completion:** 2025-12-01
- **Final completion:** 2026-06-01
- **Target enrollment:** 90 (ESTIMATED)
- **Last updated:** 2024-07-03

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06478433

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06478433, "Study on the Efficacy and Safety of a Device for Post-op Recovery in Pediatric Adenectomy/Adenotonsillectomy.". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT06478433. Licensed CC0.

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