Is Routine Cervical Dilatation Necessary During Elective Caesarean Section? A Randomised Controlled Trial
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|ClinicalTrials.gov Identifier: NCT01954719|
Recruitment Status : Unknown
Verified September 2013 by Bakirkoy Dr. Sadi Konuk Research and Training Hospital.
Recruitment status was: Recruiting
First Posted : October 7, 2013
Last Update Posted : October 7, 2013
|Condition or disease||Intervention/treatment||Phase|
|Failure of Cervical Dilatation Complications; Cesarean Section Wound Infection, External Causes of Morbidity and Mortality||Procedure: cervix dilated after surgery Procedure: control group||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||200 participants|
|Intervention Model:||Crossover Assignment|
|Masking:||None (Open Label)|
|Official Title:||Is Routine Cervical Dilatation Necessary During Elective Caesarean Section? A Randomised Controlled Trial|
|Study Start Date :||November 2012|
|Estimated Primary Completion Date :||December 2013|
|Estimated Study Completion Date :||January 2014|
Experimental: cervix dilated after surgery
Digital cervical dilatation performed by surgeon
Procedure: cervix dilated after surgery
The surgeon inserted his or her double-gloved index digit in the cervical canal to dilate it and removed the outer gloves after digital dilatation of the cervix.
Procedure: control group
surgeon not dilated cervix after surgery
No Intervention: control group
cervix not dilated after surgery
- The primary outcome was rate of post-partum endometritis [ Time Frame: All patients in both groups were observed daily,blood count was assessed 24 h after delivery and the patients were discharged on third postoperative day if there was no infection or complication ]The post-partum care for both groups was identical, and included vital signs every four hours, discontinuation of the Foley catheter and advancement of diet on the first postoperative day. All patients in both groups were observed daily in order to assess the following variables: any sign of wound infection (erythema, swelling, discharge or tenderness), vaginal discharge, uterine consistency and height and peritoneal reaction for peritonitis. Clinical signs of urinary tract infection were checked, and urinalysis was performed. A complete blood count was assessed 24 h after delivery. The patients were discharged on third postoperative day if there was no infection or complication.
- Secondary outcomes that were analysed included wound infection, febrile morbidity and infectious morbidity. [ Time Frame: Febrile morbidity, blood loss and wound infection diagnosed at least 24 h after surgery ]Febrile morbidity was defined as a persistent fever of at least 38 celsius degree for at least 24 h after surgery and not associated with lower abdominal or pelvic tenderness and no signs of infection elsewhere. Partial or total dehiscence or presence of purulent or serous wound discharge with induration, warmth and tenderness was considered as a wound infection. Endometritis was defined here as body temperature greater than 38.5 celsius degree with concomitant foul-smelling discharge or abnormally tender uterus on bimanual examination. A diagnosis of urinary tract infection was only considered when urinary symptoms associated with significant bacteruria (> 10.000.00 organisms/mL) on culture of midstream specimen of urine were noted. Blood loss was estimated using a drop in haemoglobin concentration within 24 h after the operation.
- After elective cesarean section routine cervical dilatation is necessary? Change in post-partum maternal morbidities when compared with a similar group of women receiving intravenous antibiotics and no cervical dilatation at caesarean delivery. [ Time Frame: 24 h after surgery ]We hypothesised that routine intraoperative cervical dilatation during elective section in women receiving intravenous antibiotics would not significantly reduce post-partum maternal morbidities when compared with a similar group of women receiving intravenous antibiotics and no cervical dilatation at caesarean delivery.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01954719
|Contact: hediye dağdeviren, firstname.lastname@example.org|
|Bakirkoy Dr Sadi Konuk Training and Research Hospital||Recruiting|
|Istanbul, Bakirkoy, Turkey, 34140|
|Contact: hediye dagdeviren, md 5079872463 email@example.com|
|Principal Investigator: huseyin cengiz, md|
|Study Director:||hüseyin cengiz, md||bakirkoy dr sadi konuk training and research hospital|