McColl E
Latest
- A pilot feasibility randomised controlled trial of two behaviour change interventions compared to usual care to reduce substance misuse in looked after children and care leavers aged 12-20 years: The SOLID study
- Behaviour change interventions to reduce risky substance use and improve mental health in children in care: The SOLID three-arm feasibility RCT
- The FiCTION trial: Child oral health-related quality of life and dental anxiety across three treatment strategies for managing caries in young children
- Preoperative behavioural intervention to reduce drinking before elective orthopaedic surgery: The PRE-OP BIRDS feasibility RCT
- Cost-effectiveness of child caries management: A randomised controlled trial (FiCTION trial)
- Best-practice prevention alone or with conventional or biological caries management for 3- to 7-year-olds: The FiCTION three-arm RCT
- Letter to the editor regarding 'Impact of cigarette smoking and vaping on the outcome of full-mouth ultrasonic scaling among patients with gingival inflammation: A prospective study'
- Child caries management: A randomized controlled trial in dental practice
- Antiplatelet therapy in the primary prevention of cardiovascular disease in patients with chronic obstructive pulmonary disease: A randomised controlled proof-of-concept trial
- Brief alcohol intervention for risky drinking in young people aged 14–15 years in secondary schools: The SIPS JR-HIGH RCT
- Continuous low-dose antibiotic prophylaxis for adults with repeated urinary tract infections (AnTIC): A randomised, open-label trial
- Antiplatelet therapy in the primary prevention of cardiovascular disease in patients with chronic obstructive pulmonary disease: Protocol of a randomised controlled proof-of-concept trial (APPLE COPD-ICON 2)
- Continuous low-dose antibiotic prophylaxis to prevent urinary tract infection in adults who perform clean intermittent self-catheterisation: The AnTIC RCT
- Supporting Looked After Children and Care Leavers In Decreasing Drugs, and alcohol (SOLID): Protocol for a pilot feasibility randomised controlled trial of interventions to decrease risky substance use (drugs and alcohol) and improve mental health of look
- Autologous tolerogenic dendritic cells for rheumatoid and inflammatory arthritis
- A randomised controlled trial of losartan as an anti-fibrotic agent in non-alcoholic steatohepatitis
- An observational study of donor ex vivo lung perfusion in UK lung transplantation: DEVELOP-UK
- Antibiotic treatment for intermittent bladder catheterisation with once daily prophylaxis (the AnTIC study): Study protocol for a randomised controlled trial
- Vitamin D supplementation for 12 months in older people prevents bone loss and suppresses parathyroid hormone levels
- Antidepressant augmentation with metyrapone for treatment-resistant depression (the ADD study): A double-blind, randomised, placebo-controlled trial
- A mixed methods study to assess the feasibility of a randomised controlled trial of invasive urodynamic testing versus clinical assessment and non-invasive tests prior to surgery for stress urinary incontinence in women: The INVESTIGATE-I study
- Re: Hilton P, Bryant A, Howel D, McColl E, Buckley BS, Lucas MG, et al. Assessing professional equipoise and views about a future clinical trial of invasive urodynamics prior to surgery for stress urinary incontinence in women: A survey within a mixed methods feasibility study. Neurourol Urodyn. 2012;31(8):1223–30
- INVESTIGATE-I (INVasive Evaluation before Surgical Treatment of Incontinence Gives Added Therapeutic Effect?): A mixed-methods study to assess the feasibility of a future randomised controlled trial of invasive urodynamic testing prior to surgery for stress urinary incontinence in women
- Vitamin D supplementation in older people (VDOP): Study protocol for a randomised controlled intervention trial with monthly oral dosing with 12,000 IU, 24,000 IU or 48,000 IU of vitamin D3
- Assessing professional equipoise and views about a future clinical trial of invasive urodynamics prior to surgery for stress urinary incontinence in women: A survey within a mixed methods feasibility study