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Quantifying adhesive residue on skin: An in vivo comparison of five maxillofacial prosthetic adhesives and their failure modes

A comparative assessment of adhesive residues on the skin following the removal of extraoral silicone prostheses: An in vivo study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112264
Enrollment
5
Registered
2026-06-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Secure Adhesive Regular
Pros-Aide Adhesive: Five commercially available maxillofacial prosthetic adhesives were applied to standardized silicone strips. The primary outcome measure was the percentage of adhesive residue rema

Sponsors

Amrita Vishwa Vidyapeetham Health Sciences Campus Kochi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Healthy volunteers aged 18 to 30 years Willingness to participate and provide written informed consent No history of skin disease or adhesive allergy

Exclusion criteria

Exclusion criteria: Age: under 18 On medications that modify the skin or immune system Recent skin trauma or surgery Existing systemic condition Existing skin disease Pregnant and lactating ladies Known allergic to adhesives and/or silicone Skin hypersensitivity Participation in other clinical trials

Design outcomes

Primary

MeasureTime frame
- Percentage of adhesive residue remaining on skin after adhesive removalTimepoint: 8 hours

Secondary

MeasureTime frame
Failure modeTimepoint: 8 hours;Comparison between silicone-based and water-based adhesivesTimepoint: 8 hours;Cleanability assessmentTimepoint: 8 hours

Countries

India

Contacts

Public ContactDr Jaini JL

Amrita school of dentistry

jainijl@dental.amrita.edu9447461776

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026