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Recommendation ID IPG579/1 Question Further research, preferably in the form of randomised controlled trials, should assess the effect
Recommendation ID IPG505/1 Question Further research should focus on the extended use of telemetric adjustable pulmonary artery banding
Recommendation ID IPG509/1 Question Further research should include clear documentation of patient selection and of all complications.
Further research should include details of patient selection and report longer term outcomes.
Recommendation ID IPG777 Question Further research should include details of patient selection and report longer term outcomes. Any
Recommendation ID IPG642/1 Question Further research should include details of patient selection, durability and the incidence of complications
Recommendation ID IPG773 Question Further research should report: Any explanatory notes(if applicable) details of patient
Recommendation ID IPG771 Question Further research should report details of patient selection, duration of the effect (including whether
Recommendation ID IPG643/1 Question Further research should report details of patient selection, nodule size and position, and whether
Recommendation ID TA235/1 Question Further studies on the clinical effectiveness of mifamurtide when combined with the chemotherapy typical
Recommendation ID IPG381/1 Question Further research studies into deep brain stimulation (DBS) for intractable trigeminal autonomic cephalalgias
Recommendation ID MTG46/1 Question Further evidence to address the uncertainties in the current clinical evidence,including the impact
Recommendation ID CG184/4 Question What specialist management is effective for people whose symptoms do not respond to PPIs despite optimum
Recommendation ID CG184/5 Question What specialist investigations should be conducted to exclude a diagnosis of functional dyspepsia in
Recommendation ID CG128/2 Question Gathering information in schools or nurseries:- Does routine additional information from educational
Recommendation ID DG22/3 Question Further research is recommended on clinical outcomes associated with using the ELISA kits (LISA-TRACKER