Abstract
Study design is a crucial compound of the clinical trial. If a study is not well controlled or the appropriate study population is not chosen, it might not be possible to identify efficaciousness of an adjuvant for a reduction of postoperative adhesions. There is probably no one protocol that is most appropriate for all adjuvants; protocols must be individualized based on unique characteristics of the products and the manner in which they are to be used.
Original language | English (US) |
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Pages (from-to) | 489-492 |
Number of pages | 4 |
Journal | Infertility and Reproductive Medicine Clinics of North America |
Volume | 14 |
Issue number | 3 |
State | Published - Jul 2003 |
Externally published | Yes |
ASJC Scopus subject areas
- Obstetrics and Gynecology