Watson 1988.
Methods |
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Participants |
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Interventions | Treatment group
Control group
Co‐interventions
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Outcomes |
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Notes |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Not reported |
Allocation concealment (selection bias) | Low risk | Randomly allocated by sealed envelopes |
Blinding of participants and personnel (performance bias) All outcomes | High risk | No blinding and lack of blinding could influence patient management |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Laboratory results and bone histology assessed by investigator unaware of treatment |
Incomplete outcome data (attrition bias) All outcomes | Low risk | All patients completed study |
Selective reporting (reporting bias) | Low risk | All relevant outcomes reported |
Other bias | High risk | Supported by Leo laboratories |
AKI ‐ acute kidney injury; ALP ‐ alkaline phosphatase; AKI ‐ acute kidney injury; BMD ‐ bone mineral density; Ca ‐ serum calcium; Ca x P ‐ calcium‐phosphorus product; CAPD ‐ continuous ambulatory peritoneal dialysis; CCPD ‐ continuous cycling peritoneal dialysis; CKD ‐ chronic kidney disease; CrCl ‐ creatinine clearance; DHT ‐ dihydrotachysterol; eGFR ‐ estimated glomerular filtration rate; HD ‐ haemodialysis; HVSDS ‐ height velocity standard deviation score; IP ‐ intraperitoneal; IV ‐ intravenous; K ‐ serum potassium; M/F ‐ male/female; PD ‐ peritoneal dialysis; PTH ‐ parathyroid hormone; SLE ‐ systemic lupus erythrocytosis; RCT ‐ randomised controlled trial; rhGH ‐ growth hormone; RRT ‐ renal replacement therapy; SDS ‐ standard deviation score