A systematic review of clinical trials registered on ClinicalTrials.gov reveals significant gaps in research and intervention strategies for recurrent spontaneous abortion (RSA). The analysis, encompassing 138 trials, highlights a concentration on drug interventions, particularly anticoagulants, for unexplained RSA (URSA), suggesting a need for more diverse approaches.
Trial Characteristics
The study, published in Frontiers in Endocrinology, examined trials registered up to March 2, 2024. Of the 138 trials identified, 72 (52.17%) were classified as intervention trials, while 66 (47.83%) were observational. A significant portion (48.55%) of the studies enrolled 100 or fewer participants, and the majority focused exclusively on female participants. Geographically, Asia hosted the highest number of trials (46, 33.33%), followed by Europe (36, 26.09%), Africa (29, 21.01%), and America (13, 9.42%).
Focus on Unexplained RSA and Drug Interventions
The analysis indicated that 61 trials (44.20%) specifically targeted individuals with URSA. Among intervention types, drug interventions were predominant (49, 62.82%), with a notable increase in behavioral intervention trials also observed. The emphasis on drug interventions, particularly anticoagulants, suggests a prevailing hypothesis regarding the role of coagulation disorders in RSA, but also highlights a potential lack of exploration into other potential etiologies and therapeutic strategies.
Implications for Future Research
The authors suggest that current research efforts in RSA are insufficient for advancing prevention and treatment strategies. The concentration on URSA and drug interventions, particularly anticoagulants, may overlook other contributing factors and potential therapeutic avenues. The review underscores the need for more comprehensive and diversified research approaches to address the complex challenges of RSA. Further research should explore a broader range of interventions and consider the diverse underlying causes of RSA to improve outcomes for affected women.