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Showing 5581 to 5595 of 7707 results

  1. Further research including the use of observational data from registries should provide information on patient selection, safety outcomes, quality of life, long-termoutcomes and the position of the procedure in the treatment pathway. NICE may update the guidance on publication of further evidence.

    Recommendation ID IPG598/1 Question Further research including the use of observational data from registries should provide information

    Research recommendation
    Published
    18 October 2018

  2. Further research in low-intensity pulsed ultrasound to promote healing of fresh fractures at high risk of non-healing should include details of patient selection, fracture site, and risk factors and comorbidities that delay fracture healing.

    Recommendation ID IPG622/1 Question Further research in low-intensity pulsed ultrasound to promote healing of fresh fractures at high risk

    Research recommendation
    Published
    11 December 2018

  3. Further research into arthroscopic radiofrequency chondroplasty of the knee should clearly document patient selection and the types of chondral defects being treated. More evidence on long-term outcomes would be useful.

    Recommendation ID IPG493/1 Question Further research into arthroscopic radiofrequency chondroplasty of the knee should clearly document

    Research recommendation
    Published
    9 June 2015

  4. Further research in people who could have conventional cardiac pacemaker implantation should report the patient selection criteria and compare leadless pacemakers with conventional pacemakers. Follow-up should be for at least 5 years and outcomes should include adverse events, symptom relief, quality of life and device durability in the long-term.

    Recommendation ID IPG626/1 Question Further research in people who could have conventional cardiac pacemaker implantation should report

    Research recommendation
    Published
    12 December 2018

  5. Further research in superior rectal artery embolisation for haemorrhoids should report details of patient selection, and follow-up efficacy (including symptom relief), need for subsequent treatments, quality of life and safety outcomes for at least 1 year.

    Recommendation ID IPG627/1 Question Further research in superior rectal artery embolisation for haemorrhoids should report details of patient

    Research recommendation
    Published
    12 December 2018

  6. Further research into endoscopic radiofrequency therapy of the anal sphincter for faecal incontinence should clearly define the patient groups being treated. It should also report the clinical impact in terms of quality of life and long-term outcomes. NICE may review the procedure on publication of further evidence.

    Recommendation ID IPG393/1 Question Further research into endoscopic radiofrequency therapy of the anal sphincter for faecal incontinence

    Research recommendation
    Published
    9 June 2015

  7. Further research into extraurethral (noncircumferential) retropubic adjustable compression devices for stress urinary incontinence in women should include detailed safety outcomes, long-term results and patient-reported outcome measures. NICE may update the guidance on publication of further evidence.

    Recommendation ID IPG576/1 Question Further research into extraurethral (noncircumferential) retropubic adjustable compression devices

    Research recommendation
    Published
    15 May 2017

  8. Further research into hand allotransplantation should include data on long-term functional outcomes, and any occurrence of malignancy associated with long-term immunosuppression should be published. NICE may review this procedure on publication of further evidence.

    Recommendation ID IPG383/1 Question Further research into hand allotransplantation should include data on long-term functional outcomes

    Research recommendation
    Published
    9 June 2015

  9. Further research into implantation of a shock or load absorber for mild to moderate symptomatic medial knee osteoarthritis should include comparative studies against existing forms of management. Studies should record patient selection, functional outcomes, quality of life and complications. They should also report the nature and timing of any further surgery on the knee and the effect of removing the device. A minimum follow-up period of 2–3 years is needed. NICE may update the guidance on publication of further evidence.

    Recommendation ID IPG512/1 Question Further research into implantation of a shock or load absorber for mild to moderate symptomatic medial

    Research recommendation
    Published
    9 June 2015

  10. Further research into joint distraction for ankle osteoarthritis should include comparative studies against the natural history of the disease and against other forms of management. Studies should record patient selection, pain relief, functional outcomes, complications, and quality of life in the long term. They should also report the nature and timing of any further surgery on the ankle.Minimising loss to follow-up is of particular importance. NICE may update the guidance on publication of further evidence.

    Recommendation ID IPG538/1 Question Further research into joint distraction for ankle osteoarthritis should include comparative studies

    Research recommendation
    Published
    25 January 2016

  11. Further research into joint distraction for knee osteoarthritis without alignment  correction should include comparative studies against existing forms of management. Studies should record patient selection, joint space measurements in the medium to long term, functional outcomes, quality of life and complications. They should also report the nature and timing of any further surgery on the knee. NICE may update the guidance on publication of further evidence.

    Recommendation ID IPG529/1 Question Further research into joint distraction for knee osteoarthritis without alignment correction should

    Research recommendation
    Published
    9 October 2015

  12. Further research into open reduction of slipped capital femoral epiphysis should clearly describe details of clinical presentation (for example, Loder classification), the degree of slip, its stability, and the surgical technique used; including whether surgical dislocation of the hip was done. Outcomes from 2 years onwards should include degree of correction, occurrence of avascular necrosis and need for subsequent hip surgery (and its timing).

    Recommendation ID IPG511/1 Question Further research into open reduction of slipped capital femoral epiphysis should clearly describe details

    Research recommendation
    Published
    9 June 2015

  13. Further research into percutaneous atherectomy of femoropopliteal arterial lesions with plaque excision devices should take the form of well-conducted trials, which should define patient selection, treatment protocols and location and types of arterial lesions treated, and report long-term patency outcomes. NICE may review this procedure on publication of further evidence.

    Recommendation ID IPG380/1 Question Further research into percutaneous atherectomy of femoropopliteal arterial lesions with plaque excision

    Research recommendation
    Published
    9 June 2015

  14. Further research into whether concomitant dacarbazine enhances the clinical effectiveness of ipilimumab would be encouraged because it could provide information for future treatment strategies, as would more data on the relative effectiveness of ipilimumab when given as a first-line or second-line treatment.

    Recommendation ID TA319/2 Question Further research into whether concomitant dacarbazine enhances the clinical effectiveness of ipilimumab

    Research recommendation
    Published
    9 June 2015

  15. Further research into the analytical and clinical validity of the enzyme-linked immunosorbent assay (ELISA) kits (LISA-TRACKER, IDKmonitor and Promonitor) is recommended, specifically on:- the best methods to measure tumour necrosis factor (TNF)-alpha-inhibitor levels in the presence of antibodies to TNF-alpha inhibitors- developing primary reference standards- the accuracy for predicting clinical state- clinically meaningful thresholds.

    Recommendation ID DG22/1 Question Further research into the analytical and clinical validity of the enzyme-linked immunosorbent assay (ELISA)

    Research recommendation
    Published
    21 March 2016