Home » Trials » SLCTR/2013/007 » Progress Reports
Date Modified
2013-12-26
Period
12/months
Report Summary
After the required number of the clinical subjects specified in the sample size calculation had been recruited, and the analysis of the data clearly indicated that the new method using free flow of normal saline within the Veress needle at the time of laparoscopic entry, demonstrated better efficacy and safety compared to the existing gold standard method.