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Radio surgery versus 80% phenol for toe nail matrix ablation: a randomised comparison study

Radio surgery versus 80% phenol for toe nail matrix ablation: a randomised comparison study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN32883274
Enrollment
60
Registered
2006-09-29
Start date
2005-09-01
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Surgery: Toenail matrix ablation Surgery Toenail matrix ablation

Interventions

60 participants (patients who have been referred for nail surgery) will be allocated an ID number. 30 randomised to 80% phenol and 30 will receive radio surgery technique for nail matrix ablation usin

Sponsors

Record Provided by the NHSTCT Register - 2006 Update - Department of Health
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Subjects will be males and females 2. Aged 18-80 years 3. They will be individuals referred to the podiatry department at the Royal Devon and Exeter Hospital (Heavitree) for nail surgery under local anaesthesia 4. They will present with a condition indicating the need for nail surgery including the following conditions: 4.1 Ingrowing toenail 4.2 Involuted nail 4.3 Fungal infection of the nail 4.4 Thickening of the nail 4.5 Severe nail hypertrophy 5. Each subject must be able to attend for follow-up visits including a 6-month visit and be able to provide informed consent 6. Participants will be happy to have their toe photographed and will be happy to be contacted by telephone after 1 year

Exclusion criteria

Exclusion criteria: 1. Fitted with a pacemaker, artificial heart valve, artificial joints or any other type of implant because these are contra-indications to radiosurgery 2. Subungual exostosis because treatment other than nail surgery is required for this condition 3. Contraindication to anaesthesia or the procedure according to standard guidelines 4. Pregnancy or breastfeeding 5. Unable to give informed consent 6. Inadequate blood supply to the foot or toe

Design outcomes

Primary

MeasureTime frame
Healing time of the wound (to the nearest week). Pain experienced at each return visit following surgery measured using a visual scale, post-operative infection incidence measured by clinical signs and symptoms, nail regrowth incidence measured by clinical signs and symptoms, time to nail regrowth following surgery.

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026