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. 2014 Jul 22;3:79. doi: 10.1186/2046-4053-3-79

Table 1.

Summary of included studies

  Study design Population Size Antibiotics Control Intervention Analysis Key findings
[26]
RCT
Acute salpingitis or PID
40
Co-amoxiclav 1 g three times daily doxycycline 200 mg once daily intravenously for 5 days followed by co-amoxiclav 500 mg three times daily for 15 days and doxycycline 200 mg once daily for 21 days
No NSAID
Piroxicam 20 mg/day from day 3 post-operation for 25 days
Per protocol
Tubal patency: in severe PID, bilateral patency was seen in 1/7 (14.2%) of placebo group versus 7/9 (77.8%) of intervention group (P = 0.02, Fisher’s exact test)
Confirmed by laparoscopy
Residual adhesions: in severe PID, more patients in intervention group had no residual adhesions, 6/9 (66.7%), versus control group, 1/7 (14.3%) (P = 0.06, Fisher’s exact test)
No difference between arms in tubal patency or residual adhesions for mild or moderate PID
[27] RCT Mild acute PID
42 Tetracycline 500 mg four times daily for 10 days Placebo Fentiazac 200 mg twice daily for 7 days Intention to treat Suprapubic pain: resolution of pain occurred by day 7 in 9/21 (43%) of patients in the intervention group versus 5/21 (24%) in the control group (P = 0.2, χ square)
Clinical diagnosis
Reduction in overall signs and symptoms: greater reduction in average score for severity of signs and symptoms in the intervention compared with the placebo group (figures providing the basis of the calculation not provided)
Nausea reported in 4/21 patients receiving fentiazac (1 discontinuation) versus 2/21 in the control group (no discontinuations)

NSAID nonsteroidal anti-inflammatory drug; PID pelvic inflammatory disease; RCT randomized controlled trial.