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Table 1 Trial characteristics

From: The efficiency of risedronate in reducing bone resorption after total hip arthroplasty: a meta-analysis of randomized control trials at a minimum of 6 months’ follow-up

Studies

Year

Reference type

Cases (risedronate /C)

Mean age (risedronate /C)

Female%

Risedronate group

Control group

Follow-up

Kinov

2005

RCT

12/12

58.3/56

62.5%

35 mg risedronate

No treatment

A minimum of half year

Yamasaki

2006

RCT

19/21

66.8/66.7

90%

2.5 mg/day orally

Placebo

A minimum of half year

Skoldenberg

2011

RCT

36/37

61.2/60.3

59%

35 mg risedronate

Placebo

A minimum of 1 year

Muren

2015

RCT

30/31

62.5/60.8

38%

35 mg risedronate

Placebo

A minimum of 4 years

  1. RCT randomized controlled trial, C control