El‐Sefi 1986 A.
Methods | Randomised controlled trial. Randomisation based on a table of random numbers. Patient blinded. Unclear blinding of surgeon and outcome assessor. | |
Participants | 480 eligible patients. 80 patients excluded after randomisation. 400 enrolled in the study. Patients with perforated appendix were excluded after randomisation. The study has 4 subgroups (see El‐Sefi 1986 B & C). In El‐Sefi 1986 A 200 patients enrolled in the study. | |
Interventions | Treatment group: Metronidazole 500 mg IV preoperatively and eight‐hourly for the next 3 days. (When the patient tolerated oral medication converted to 250 orally) and Cefazolin 500 mg i.v preoperatively and eight‐hourly for the next 3 days. (When the patient tolerated oral medication converted to 250 orally). Placebo group: Not specified, same regime as above | |
Outcomes | Wound infection (Presence of pus or a purulent exudate of the wound). | |
Notes | No comments on drain treatment. Wrote to author to specify subgrouping on drop‐outs. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Allocation concealment? | Low risk | A ‐ Adequate |