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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02696837
Other study ID # PIRS002
Secondary ID
Status Completed
Phase N/A
First received February 22, 2016
Last updated May 28, 2016
Start date March 2016
Est. completion date May 2016

Study information

Verified date May 2016
Source Maltepe University
Contact n/a
Is FDA regulated No
Health authority Turkey: Ethics Committee
Study type Interventional

Clinical Trial Summary

In prospective, safety-control study; children undergoing laparoscopic inguinal hernia repair using PIRS (Percutaneous Internal Ring Suturing) method will be randomly assigned into four groups. Gr 1: Endotracheal intubation and muscle relaxant, Gr 2: Endotracheal Intubation without muscle relaxant, Gr 3: Proseal Laryngeal Mask Airway without muscle relaxant, Gr 4: Proseal Laryngeal Mask Airway with subparalytic does muscle relaxant. Apart from standard monitorization, all patients' intragastric pressures will also be monitored. Patients' age at presentation, gender, time of surgery, time of anesthesia, intragastric pressure, intraabdominal pressure, intraoperative findings and complications will be noted and compared between groups.


Description:

In this prospective, safety-control study; children undergoing laparoscopic inguinal hernia repair using PIRS (Percutaneous Internal Ring Suturing) method will be randomly assigned into four groups.

Gr 1: Endotracheal intubation and muscle relaxant, Gr 2: Endotracheal Intubation without muscle relaxant, Gr 3: Proseal Laryngeal Mask Airway without muscle relaxant, Gr 4: Proseal Laryngeal Mask Airway with subparalytic does muscle relaxant.

Apart from standard monitorization, all patients' intragastric pressures will also be monitored. Patients' age at presentation, gender, time of surgery, time of anesthesia, intragastric pressure, intraabdominal pressure, intraoperative findings and complications will be noted and compared between groups.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date May 2016
Est. primary completion date May 2016
Accepts healthy volunteers No
Gender Both
Age group N/A to 18 Years
Eligibility Inclusion Criteria:

- Children aged 0-18 years

- Diagnosed with inguinal hernia or communicating hydrocele

- Due to undergo laparoscopic inguinal hernia repair

Exclusion Criteria:

- Previous abdominal surgery

- Comorbidities that will effect surgical time, time under anesthesia, intragastric pressure and abdominal pressure

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor)


Intervention

Device:
ETT

Proseal LMA

Drug:
Rocuronium

Other:
No Muscle Relaxant

Drug:
Rocuronium


Locations

Country Name City State
Turkey Maltepe University Hospital Istanbul

Sponsors (3)

Lead Sponsor Collaborator
Maltepe University Hisar Intercontinental Hospital, Pendik State Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (5)

Aydogmus MT, Turk HS, Oba S, Unsal O, Sinikoglu SN. Can Supreme™ laryngeal mask airway be an alternative to endotracheal intubation in laparoscopic surgery? Braz J Anesthesiol. 2014 Jan-Feb;64(1):66-70. doi: 10.1016/j.bjane.2012.12.008. Epub 2013 Dec 3. — View Citation

Chen BZ, Tan L, Zhang L, Shang YC. Is muscle relaxant necessary in patients undergoing laparoscopic gynecological surgery with a ProSeal LMA™? J Clin Anesth. 2013 Feb;25(1):32-5. doi: 10.1016/j.jclinane.2012.06.004. Epub 2012 Nov 2. — View Citation

Liu HC, Tao WK, Zeng RF, ShangGuang WN, Li J, Huang WG, Dong ZL, Wang X, Lian QQ. Dose requirements of remifentanil for intubation in nonparalyzed Chinese children. Paediatr Anaesth. 2014 May;24(5):505-9. doi: 10.1111/pan.12354. Epub 2014 Feb 7. — View Citation

Ozdamar D, Güvenç BH, Toker K, Solak M, Ekingen G. Comparison of the effect of LMA and ETT on ventilation and intragastric pressure in pediatric laparoscopic procedures. Minerva Anestesiol. 2010 Aug;76(8):592-9. Epub 2010 Jun 18. — View Citation

Thomas DT, Göcmen KB, Tulgar S, Boga I. Percutaneous internal ring suturing is a safe and effective method for the minimal invasive treatment of pediatric inguinal hernia: Experience with 250 cases. J Pediatr Surg. 2015 Dec 11. pii: S0022-3468(15)00824-6. doi: 10.1016/j.jpedsurg.2015.11.024. [Epub ahead of print] — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Surgery Time Time from skin prep to last suture Intraoperative Yes
Primary Time Under Anesthesia Time from induction to moderate Alderete score of 9 or above Intraoperative Yes
Primary Intragastric Pressure Intraoperative continuous monitoring Yes
Primary Intraabdominal Pressure Intraoperative continuous monitoring Yes
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