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A comparison study of pain perception during microfocused ultrasound procedure between topical anesthesia and combined topical anesthesia with forced air cooling

A comparison study of pain perception during microfocused ultrasound procedure between topical anesthesia and combined topical anesthesia with forced air cooling

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220225003
Enrollment
21
Registered
2022-02-25
Start date
2021-11-19
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Heathy person Anesthesia, Lidocaine, Pain score, Prilocaine, Tightening

Interventions

Topical anesthesia (5%/5% lidocaine-prilocaine
Galentic Pharma, Navi Mumbai, India) was applied to the studied area with an occlusive dressing for 30 minutes before microfocused procedure. Forced air cooling was delivered to the assigned side of t
Galentic Pharma, Navi Mumbai, India) was applied to the studied area with an occlusive dressing for 30 minutes before microfocused procedure.
Experimental Other,No Intervention Drug
Combined topical anesthesia with forced air cooling ,Topical anesthesia

Sponsors

Division of Dermatology, Department of medicine, Faculty of Medicine, Ramathibodi hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Healthy subjects older than 18-year-old

Exclusion criteria

Exclusion criteria: The exclusion criteria included pregnancy or active breastfeeding, active skin diseases, history of surgery at the experimental sites within 6 months, metal implantation at the experimental sites, and allergy to local anesthesia

Design outcomes

Primary

MeasureTime frame
Pain score After performing 4.5 MHz, 4.5 mm transducer (10 lines, 0.9 J) (T1a), after performing 7 MHz, 3.0 mm transducer (10 lines, 0.3 J) (T1b), and after the entire procedure (T2) Visual analogue scale

Secondary

MeasureTime frame
Side effect After completing the procedure Participants

Countries

Thailand

Contacts

Public ContactVasanop Vachiramon

Faculty of Medicine, Ramathibodi hospital

vasanop@gmail.com022011211

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026