Objectives: The aims of the study were to correlate
endometriosis-associated
pain, evaluated by visual analogue scale (VAS) scores, with serum levels of
etonogestrel (ENG),
levonorgestrel (LNG), CA-125 and soluble CD23 in users of the ENG implant or the 52-mg LNG-releasing intrauterine system (52 mg LNG-IUS) for up to 2 years after device placement.Methods: A randomised trial was conducted at the University of Campinas Medical School, Brazil. All participants (n = 103) had had
endometriosis-associated chronic
pelvic pain or dysmenorrhoea, or both, for more than 6 months. Participants were randomly assigned to use an ENG
implant (experimental treatment) or a 52-mg LNG-IUS (active comparator). Follow-up was conducted 6 monthly for up to 24 months after device placement. Dysmenorrhoea and chronic
pelvic pain were evaluated using a VAS and the scores were correlated with serum levels of ENG, LNG, CA-125 and soluble CD23.Results: Both
progestin-only
contraceptives significantly reduced VAS scores for dysmenorrhoea and chronic
pelvic pain and reduced serum levels of soluble CD23 (p < 0.001). Serum levels of CA-125 decreased only in the ENG implant group after 24 months' use of the device (p < 0.001). No correlation was found between
pain scores and ENG or LNG serum levels over time (p > 0.005).Conclusion: Both
contraceptives improved dysmenorrhoea and chronic
pelvic pain scores in women with
endometriosis-associated
pain and they reduced serum levels of soluble CD23; however, serum levels of CA-125 were reduced only in ENG implant users over the 24-month study period.