Safety Study of Quickclot for Bleeding Control After Adenotonsillectomy
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| ClinicalTrials.gov Identifier: NCT01863563 |
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Recruitment Status :
Completed
First Posted : May 29, 2013
Results First Posted : March 7, 2018
Last Update Posted : March 26, 2019
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Sleep Apnea, Obstructive | Device: QuickClot | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 100 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Intervention Model Description: | Quickclot |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | Hemostatic Control After Adenotonsillectomy- Open Label QuikClot Study. |
| Study Start Date : | December 2012 |
| Actual Primary Completion Date : | November 2013 |
| Actual Study Completion Date : | November 2013 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: QuickClot
QuickClot sponge will be applied for one minute each site of tonsillectomy and Adenoidectomy.
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Device: QuickClot
1 application of treatment to each tonsil/adenoid removal area |
- Total Suction Electrocautery Time Required for Hemostasis Will be Recorded as Seconds [ Time Frame: at the time of surgery, 1 hour ]After removal of the adenoids, a tonsil pack wrapped in QuikClot will be placed in the nasopharynx. The investigators will then perform tonsillectomy with the Microdebrider. A QuikClot roll will be placed in the tonsil fossa, and pressure applied via tonsil sponge for one minute. The contralateral tonsil will then be addressed with the same technique. The QuikClot adenoid pack is then removed and residual adenoidal bleeding is addressed with suction electrocautery, followed by placement of a second QuikClot adenoid pack. The tonsil rolls are sequentially removed, followed by control of residual hemostasis with suction electrocautery. A second set of tonsil rolls are placed. After adenoid pack is removed from nasopharynx and bleeding controlled, tonsil rolls are removed, followed by suction electrocautery for any residual hemostasis is performed.
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| Ages Eligible for Study: | 2 Years to 17 Years (Child) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- diagnosis of adenotonsillar hypertrophy causing obstructive sleep disorders
Exclusion Criteria:
- Patients with signs or symptoms of obstructed breathing
- recurrent pharyngitis
- history of bleeding disorder
- history of prior adenotonsillectomy
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): NCT01863563
| United States, Virginia | |
| Children's Hospital of the Kings Daughters | |
| Norfolk, Virginia, United States, 23507 | |
| Principal Investigator: | Craig Derkay, MD | EVMS Department of Otolaryngology |
| Responsible Party: | Eastern Virginia Medical School |
| ClinicalTrials.gov Identifier: | NCT01863563 |
| Other Study ID Numbers: |
version 4 September 2012 |
| First Posted: | May 29, 2013 Key Record Dates |
| Results First Posted: | March 7, 2018 |
| Last Update Posted: | March 26, 2019 |
| Last Verified: | March 2019 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
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tonsillectomy adenoidectomy obstructive sleep apnea |
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Sleep Apnea Syndromes Sleep Apnea, Obstructive Apnea Respiration Disorders Respiratory Tract Diseases |
Sleep Disorders, Intrinsic Dyssomnias Sleep Wake Disorders Nervous System Diseases |

