Hallux Rigidus, Hallux Valgus
Conditions
Keywords
Randomised controlled trial, Hallux valgus correction, Hallux rigidus correction, Tourniquet, Foot volume
Brief summary
Patients listed for hallux valgus/hallux rigidus correction surgery will be randomised to one of two treatment groups. Group 1 (standard care) will have the calf tourniquet released after wound closure. Group 2 will have the tourniquet removed five minutes before wound closure. Participants will have the volume of their operated foot measured pre-operatively and post-operatively at six weeks and three months.
Detailed description
Pneumatic tourniquets provide the benefits of better visualisation and decreased blood loss, but can also cause metabolic changes due to ischemia and compressive damage due to pressure. Surveys of foot and ankle surgeons demonstrates prevalent use of tourniquets in their clinical practice, with various patterns of use differing amongst the surgeons. Bunion surgery is one of the most common surgical procedures in foot surgery. It involves correcting the hallux valgus deformity through a combination of various osteotomy, fusion, or soft tissue procedures. Swelling after any surgery is common, but particularly so after foot surgery as gravity causes fluid to collect in the foot. With regards to recovery after surgery, patients are advised to expect to be off work for between 6-8 weeks for a sedentary occupation, and between 12-14 weeks for heavy work. Although patients have low pain levels, the foot remains swollen for an average of 3-6 months after surgery. It is usually the swelling that prevents patients from getting in to normal footwear to be able to return to work sooner. Bunion surgery is usually performed under a calf-tourniquet to create a bloodless surgical field and ensure less surgical bleeding, thereby reducing surgical time. However, use of tourniquets can lead to more swelling, increased post-operative pain and challenges in rehabilitation - all of which may affect recovery after bunion surgery. Prolonged duration of tourniquet use has been shown to cause post-operative wound healing complications, potentially attributable to local inflammation and tissue hypoxia. It is known from the studies for knee replacement surgery that tourniquet use can lead to decreased range of motion after surgery in early stage. This study will be a randomised controlled trial with two study groups. The control group will have surgery with the tourniquet remaining in situ until the wound is closed. The intervention group will have the tourniquet released after surgery, but closure will be delayed by five minutes.
Interventions
OTHERStandard care
Hallux valgus/hallux rigidus surgery with the calf tourniquet remaining in situ until the wound is closed.
OTHERTourniquet release
Hallux valgus/hallux rigidus surgery with the calf tourniquet released five minutes before the wound is closed.
Sponsors
Golden Jubilee National Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)
Masking description
Those collecting and analysis the data will be masked to the treatment groups. It is not possible to mask the participant or the care provider in this study
Intervention model description
Two randomised study groups with one having standard care and the other the intervention.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients having hallux valgus or hallux rigidus * Able to give informed consent * Able to return for follow-up
Exclusion criteria
* Patients with symptomatic peripheral vascular disease * Patients with known peripheral oedema from any cause * Patients who will also require lesser toe correction as part of the procedure * Active smokers
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Foot volume | 3 months post-operatively | The volume of the operated foot measured by water displacement (in millilitres). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| MOxFQ score | 3 months post-operatively | Manchester-Oxford Foot Questionnaire score (0-100, 100 being the most severe) |
| Foot pain assessed using a dolometer | 3 months post-operatively | Foot pain measured on a visual analogue scale (0-10, 0 being no pain & 10 being worst pain imaginable). |
| Return to work | 3 months post-operatively | Time after surgery the participant returned to work (reported in weeks since surgery) |
Countries
United Kingdom
Contacts
Primary ContactAlistair M Ewen, Ph. D.
Backup ContactKathryn Macpherson, B. Sc.
Outcome results
None listed