Safety and Efficacy Study of a Hydrogel, Applied Following Removal of Myomas During Gynecologic Surgery, Administered for the Prevention/Reduction of Postoperative Adhesion Formation

Inclusion Criteria: Preoperatively, subjects must have had: * Been scheduled for myomectomy via laparotomy or laparoscopy. * Agreed to a second-look laparoscopic procedure to assess and lyse any adhesions formed at 6 to 8 weeks following myomectomy. * Been \>=18 years of age. * Provided voluntary written informed consent. * Been willing to comply with all aspects of the treatment and evaluation schedule. Intra-operatively, subjects must have had: * Had at least one 2 cm incision length on posterior uterine surface, which may include the fundal surface. Exclusion Criteria: Preoperatively, subjects must not have had: * Been pregnant. * Had a pelvic malignancy. * Had acute pelvic inflammatory disease. * Had an immune compromised condition. * Been a participant in another clinical research study which the investigator believed could interfere with the purpose of this study. * Been given corticosteroids intra-operatively or during the course of the postoperative study follow up. Intra-operatively, subjects must not have had: * Had a pelvic malignancy. * Had a pelvic or abdominal infection. * Had acute pelvic inflammatory disease. * Received any adhesion prevention adjuvants or barriers, or peritoneal instillates containing corticosteroids, NSAIDs, or Dextran.