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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01684839
Other study ID # HB-TS-120127
Secondary ID TSCHEN411206
Status Completed
Phase N/A
First received
Last updated
Start date May 2007
Est. completion date March 2012

Study information

Verified date June 2012
Source The Second Hospital of Tangshan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Neuroma excision and digital nerve reconstruction remain the best option for the treatment of Painful Digital Neuroma (PDN). When the distal nerve end is preserved, conventional nonvascularized nerve grafting is the primary option to bridge the defect. The investigators hypothesize the pedicled nerve flap taken from the dorsal branch of the homolateral digital nerve is better than conventional methods for reconstruction of the digital nerve defect after painful neuroma resection. This study reports treatment of painful digital neuroma using a pedicled nerve flap taken from the dorsal branch of homolateral digital nerve. From May 2007 to March 2010, the patients had previous nerve injuries with or without nerve repair. The mechanisms of injury include sharp cut, avulsion and crush. The defects were between the middle of the distal phalanx and the palmar digital crease.


Description:

Our selection criteria in this study included a patient with PDN in a scarred wound bed or poor coverage, a PDN located between the middle of the distal phalanx and the palmar digital crease, and a defect of the digital nerve after neuroma resection equal to or less than 3 cm in length. The exclusion criteria included a PDN in healthy soft tissue, a digital nerve defect longer than 3 cm, injury to the course of the pedicle or the donor nerve, and a thumb neuroma. A finger with a small distal end of the digital nerve was also excluded, because neurorrhaphy was extremely difficult in this situation.


Recruitment information / eligibility

Status Completed
Enrollment 9
Est. completion date March 2012
Est. primary completion date March 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 15 Years to 55 Years
Eligibility Inclusion Criteria: - a patient with PDN in a scarred wound bed or poor coverage - a PDN located between the middle of the distal phalanx and the palmar digital crease - a defect of the digital nerve after neuroma resection equal to or less than 3 cm in length Exclusion Criteria: - a PDN in healthy soft tissue - a digital nerve defect longer than 3 cm - injury to the course of the pedicle or the donor nerve - a thumb neuroma

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Pedicled nerve flap
This nerve flap is a vascularized nerve graft

Locations

Country Name City State
China The Second Hospital of Tangshan Tangshan Hebei

Sponsors (3)

Lead Sponsor Collaborator
The Second Hospital of Tangshan Chinese PLA General Hospital, The Second Hospital of Qinhuangdao

Country where clinical trial is conducted

China, 

References & Publications (2)

Herndon JH, Eaton RG, Littler JW. Management of painful neuromas in the hand. J Bone Joint Surg Am. 1976 Apr;58(3):369-73. — View Citation

Tupper JW, Booth DM. Treatment of painful neuromas of sensory nerves in the hand: a comparison of traditional and newer methods. J Hand Surg Am. 1976 Sep;1(2):144-51. doi: 10.1016/s0363-5023(76)80008-1. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Tinel's Sign Tinel's sign was graded as the following: grade 1=none; grade 2=mild, slight tingle; grade 3=moderate, very uncomfortable; and grade 4=severe, patient unable to use hand because of any stimulation of the neuroma 20-26 months postoperatively
Primary Static 2-point Discrimination Test The Static 2-point Discrimination Test determined the minimal distance at which a subject can sense the presence of two needles. The modified American Society for Surgery of the Hand guidelines was used to stratify the 2PD measurements (excellent <6 mm; good 6-10 mm; fair 11-15 mm; poor >15 mm). The test points were at the center of the radial or ulnar portion of the finger pulp (i.e., injury side). Each area was tested 3 times with a discriminator (Ali Med, Dedham, MA). Two out of 3 correct answers were considered proof of perception before proceeding to another lower value. We stopped at 4mm as a limit of 2PD and consider this normal. The measurements were performed at a single time point at the final follow up. 20-26 months postoperatively
Secondary Cold Intolerance Severity Score (CISS) Questionnaire The maximum score was 100 and was grouped into 4 ranges (0-25; 26-50; 51-75; and 76-100), corresponding to mild, moderate, severe, and extreme severity, respectively. 20-26 months postoperatively