Kheiriyat 2016.
Study characteristics | ||
Methods | Randomised controlled trial | |
Participants | Setting: Rahzi Hospital, Ahwaz, Iran. 2015 Inclusion criteria: multiparous women with a normal‐term vaginal delivery and postpartum pain Exclusion criteria: women who were unable to be sedated and other interventions required, dystocia, prolonged labour, history of caesarean section or other abdominal surgery, any history of postpartum haemorrhage; history of underlying disease | |
Interventions | Women had their pain assessed and were randomly divided into 1 of 2 study groups (below), they received their allocated study medication 6‐hourly up to 4 times if required Experimental intervention: dill essence (Anethum graveolens extract) 1.5 mg/kg body weight, up to 4 doses (N = 54) Control/comparison: 250 mg Mefenamic acid, up to 4 doses (N = 54) |
|
Outcomes |
|
|
Notes | Funding: Ahvaz Jundishapur University of Medical Sciences No declaration of interests stated |
|
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Women were randomly divided, no other detail provided |
Allocation concealment (selection bias) | Unclear risk | Not stated |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Study not blinded |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Study not blinded |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Abstract only, total numbers randomised reported but not the number analysed. There were 54 women allocated to each group |
Selective reporting (reporting bias) | Unclear risk | No published full text or protocol available. Trial registration available but study report is abstract only |
Other bias | Unclear risk | Full article not available in English. Translation to be requested |