mesna has been researched along with Ovarian-Diseases* in 2 studies
1 trial(s) available for mesna and Ovarian-Diseases
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Chemically assisted dissection of tissues in laparoscopic excision of endometriotic cysts.
To evaluate the capacity of chemical dissection of tissues using a mucolytic substance, Mesna, in improving laparoscopic excision of endometriotic cysts.. Randomized, double-blind, controlled trial (Canadian Task Force classification I).. University-affiliated training hospital.. Forty-four women with symptomatic ovarian endometriotic cysts. Intervention. Laparoscopic excision of endometriotic cysts in 22 women with the aid of Mesna solution and in 22 with the aid of saline solution.. In comparison with saline solution, Mesna as a chemical dissector resulted in significant reductions in operating time, in difficulty encountered by the surgeon to enucleate the cysts, and in less bleeding. No differences were found in length of hospital stay, costs of surgeries, analgesic requirement, and fever. Postoperatively, patients treated with Mesna achieved more pregnancies than those treated with saline.. Chemical dissection of tissues with Mesna proved to be a safe and suitable support in laparoscopic surgery for ovarian endometriotic cysts. Topics: Adult; Combined Modality Therapy; Dissection; Double-Blind Method; Endometriosis; Female; Follow-Up Studies; Humans; Laparoscopy; Mesna; Ovarian Cysts; Ovarian Diseases; Probability; Reference Values; Risk Assessment; Severity of Illness Index; Statistics, Nonparametric; Treatment Outcome | 2003 |
1 other study(ies) available for mesna and Ovarian-Diseases
Article | Year |
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Protection against cisplatin-induced ovarian damage by the antioxidant sodium 2-mercaptoethanesulfonate (mesna) in female rats.
The hypothesis was that the administration of the antioxidant mesna (sodium 2-mercaptoethanesulfonate) during chemotherapy would protect ovaries against follicular damage.. Sprague-Dawley rats were treated with saline solution, mesna-plus-cisplatin, or cisplatin. Immunohistochemistry was used to evaluate the Müllerian inhibiting substance (MIS) positive follicles. Serum and ovarian MIS were measured with enzyme-linked immunosorbent assay and Western blot analysis, respectively. Apoptosis in ovaries was studied by terminal deoxynucleotidyl transfer biotin-d UTP nick end labeling (TUNEL) assay.. Immunofluorescence staining for MIS was higher in preantral follicles in the mesna-plus-cisplatin group. The ovarian and serum MIS levels were higher in the mesna-plus-cisplatin than in the cisplatin alone group. There were no differences statistically in the TUNEL and the ovarian cyst analyses.. Mesna, which was used at the time of cisplatin administration, protected ovaries against damage. The data that are presented challenge the existing clinical paradigm that gonadotropin-releasing hormone agonists represent the only medical method for the protection of ovaries during chemotherapy. Alternative medical means to protect ovaries during chemotherapy may be achievable. Topics: Animals; Anti-Mullerian Hormone; Antineoplastic Agents; Antioxidants; Blotting, Western; Cisplatin; Enzyme-Linked Immunosorbent Assay; Female; Follicle Stimulating Hormone; Immunohistochemistry; Mesna; Ovarian Diseases; Ovarian Follicle; Ovary; Rats; Rats, Sprague-Dawley | 2008 |