Trial Outcomes & Findings for Study on Wood-plastic Composite for Circumferential Casting (NCT NCT01493167)

NCT ID: NCT01493167

Last Updated: 2017-07-05

Results Overview

Efficient casting conduc ted with Novel Woodcast material

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

97 participants

Primary outcome timeframe

1 - 6 weeks

Results posted on

2017-07-05

Participant Flow

Participant milestones

Participant milestones
Measure
Limb Casting/Splinting
Patient age 0-90 years. Patient treatment requires extremity immobilization limb casting/splinting: ankle and arm cast
Overall Study
STARTED
97
Overall Study
COMPLETED
97
Overall Study
NOT COMPLETED
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Study on Wood-plastic Composite for Circumferential Casting

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Woodcast Circular System Casts
n=97 Participants
Operatively treated adult patients needing a post-operative Circular Woodcast scaphoid-type cast
Age, Categorical
<=18 years
0 Participants
n=5 Participants
Age, Categorical
Between 18 and 65 years
85 Participants
n=5 Participants
Age, Categorical
>=65 years
12 Participants
n=5 Participants
Sex: Female, Male
Female
59 Participants
n=5 Participants
Sex: Female, Male
Male
38 Participants
n=5 Participants
Region of Enrollment
Finland
97 participants
n=5 Participants

PRIMARY outcome

Timeframe: 1 - 6 weeks

Efficient casting conduc ted with Novel Woodcast material

Outcome measures

Outcome measures
Measure
Limb Casting/Splinting
n=97 Participants
Patient age 0-90 years. Patient treatment requires extremity immobilization limb casting/splinting: ankle and arm cast
Efficient Casting With Woodcast Circular System
90 participants

Adverse Events

Limb Casting/Splinting

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Dr Nina Linfors

Helsinki University Hospital

Phone: 358 9 4711

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place