Meta AnalysisID 548
水蛭治疗骨关节炎 [Cochrane方案]
CRD42015017418
To assess the benefits and harms of leeches compared with placebo, no intervention or any other active treatment in people with osteoarthritis.
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Record Fields
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- Meta Analysis Id
- 548
- Evidence Id
- 9106
- Core Evidence Id
- 9106
- Source Meta Analysis Id
- 527
- Herb2 Meta Analysis Id
- HBMA000527
- Crd Id
- CRD42015017418
- Title
- Leeches (Hirudinea) for osteoarthritis [Cochrane Protocol]
- Review Question
- To assess the benefits and harms of leeches compared with placebo, no intervention or any other active treatment in people with osteoarthritis.
- Study Type Included
- Randomised controlled trials (RCTs) and controlled clinical trials. Studies may be single-blind, double-blind, triple-blind or unblinded (i.e. ‘open label’).
- Condition Being Studied
- The Cochrane Musculoskeletal Group
- Participant
- Participants will be persons of any age with clinically- or radiologically-confirmed primary osteoarthritis.
- Animal
- Human Disease Modelled
- Intervention
- We will consider studies for inclusion where: any leech species is administered to a human host; in any dose (i.e. number of applied leeches, periodicity of exposure); and at any anatomical site.</ul> Leech-derived molecular products are outside the scope of this review, and are not included. Control The control group will receive placebo (i.e. sham leech exposure), no treatment, or any other active intervention.
- Comparator Control
- The control group will receive placebo (i.e. sham leech exposure), no treatment, or any other active intervention.
- Main Outcome
- Major outcomes Pain (see Appendix 6 for our proposed hierarchy of data extraction). Function (see Appendix 7 for our proposed hierarchy of data extraction). Radiographic joint structure changes (see Appendix 8 for our proposed hierarchy of data extraction). Change in Quality of Life score. Number of participants experiencing any adverse event. Number of participants experiencing serious adverse events, defined as events resulting in hospitalisation, persistent or significant disability, congenital abnormality or birth defect in offspring, or other life-threatening event or death (European Commission 2010). Dropouts (all-cause study withdrawal, number of participants withdrawing because of adverse effects). If pain or function outcomes are reported at several time points, we will extract the measure at the end of the trial or at a maximum of three months after termination of therapy, whichever came first. Minor outcomes Number of participants experiencing non-serious local adverse events (e.g. pain, itching, infection). Number of participants experiencing non-serious systemic adverse events (e.g. fever, headache, confusion). We will report the above secondary outcomes as additional tables in our review, if appropriate.
- Outcome Measure
- Additional Outcome
- Number of participants experiencing non-serious local adverse events (e.g. pain, itching, infection). Number of participants experiencing non-serious systemic adverse events (e.g. fever, headache, confusion).
- Study Method
- Keyword
- Animals; Leeches; Leeching; Humans; Osteoarthritis
- Contact
- Ashley M Croft [email protected]
- Organisational Affiliation
- The Cochrane Collaboration http://www.cochrane.org/
- Funding Source
- None specified
- Other Selection Criteria
- Final Publication
- Same Topic Review
- Published Protocol
- Review Type
- Language
- English
- Country
- England
- Review Stage
- Review Ongoing
- First Submission Date
- Registration Date
- 2015-03-09
- Anticipated Start Date
- 2014-02-15
- Anticipated Completion Date
- 2016-02-15
- Title Cn
- 水蛭治疗骨关节炎 [Cochrane方案]
- Title En
- Leeches (Hirudinea) for osteoarthritis [Cochrane Protocol]
- Bilingual Status
- complete