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Combined laparoscopic surgery and pentoxifylline therapy for treatment of endometriosis-associated infertility: A preliminary trial

机译:腹腔镜手术和己酮可可碱联合治疗子宫内膜异位症相关不育的初步研究

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BACKGROUND: Surgical treatment has modest efficacy for the treatment of infertility associated with early-stage endometriosis. Immunomodulation with pentoxifylline is considered as a new strategy potentially useful in treating endometriosis. Thus, this study investigated the usefulness of combined laparoscopic surgery and pentoxifylline therapy in the treatment of infertility associated with minimal to mild endometriosis. METHODS: A prospective, randomized, controlled blind trial was conducted. Patients entered the study immediately after laparoscopic surgery and were randomly assigned to the treatment with either oral pentoxifylline (800 mg/day) (pentoxifylline group, n = 51) or an oral placebo (placebo group, n = 53). Patients were then observed for pregnancy for 6 months. RESULTS: Among 98 patients finally considered in the evaluation of the results, the 6 month overall pregnancy rates were 28 and 14% in the pentoxifylline and placebo groups, respectively. Thus, an absolute difference of 14% (95% CI -2 to 30) (Chi-squared test, P = 0.1) in the cumulative probability of pregnancy in 6 months after laparoscopic surgery in patients receiving pentoxifylline versus placebo post-operatively was observed. CONCLUSION: Our findings provide preliminary clinical evidence to suggest the new experimental treatment approaches, toward endometriosis, that are based on immunomodulation deserve further attention. Well-designed multicenter trials are warranted to confirm or refute our results. The ClinicalTrials.gov Identifier is NCT00632697.
机译:背景:外科手术治疗与早期子宫内膜异位症相关的不育症的疗效不高。己酮可可碱的免疫调节被认为是一种潜在的治疗子宫内膜异位症的新策略。因此,本研究调查了腹腔镜手术和己酮可可碱联合疗法在治疗轻度至轻度子宫内膜异位症相关的不孕症中的作用。方法:进行了一项前瞻性,随机,对照盲法试验。患者在腹腔镜手术后立即进入研究,并随机分配接受口服己酮可可碱(800 mg /天)(己酮可可碱组,n = 51)或口服安慰剂(安慰剂组,n = 53)进行治疗。然后观察患者怀孕6个月。结果:在最终评估结果的98位患者中,己酮可可碱组和安慰剂组的6个月总妊娠率分别为28%和14%。因此,观察到接受己酮可可碱和安慰剂的患者在腹腔镜手术后6个月内的累积妊娠概率绝对差异为14%(95%CI -2至30)(卡方检验,P = 0.1)。 。结论:我们的发现提供了初步的临床证据,表明基于免疫调节的针对子宫内膜异位的新实验治疗方法值得进一步关注。设计良好的多中心试验必须确认或反​​驳我们的结果。 ClinicalTrials.gov标识符为NCT00632697。

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