Chronic Rhinosinusitis (Diagnosis) Clinical Trial
Official title:
The Effect of Intranasal Irrigation With Adrenaline Solution on Intraoperative Visualization and Bleeding During Functional Endoscopic Sinus Surgery
NCT number | NCT04551703 |
Other study ID # | 221 |
Secondary ID | |
Status | Completed |
Phase | Phase 1 |
First received | |
Last updated | |
Start date | July 1, 2016 |
Est. completion date | August 11, 2020 |
Verified date | September 2020 |
Source | Jordan University of Science and Technology |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Intranasal irrigation with normal saline is routinely used in sinus surgery to clean the tip of the nasal endoscope and clear the surgical field from blood. The purpose of this study is to evaluate the difference in the surgical visualization, surgeon satisfaction and total blood loss when intraoperative irrigation was performed with a solution of normal saline with adrenaline as compared to irrigation with normal saline alone in FESS.
Status | Completed |
Enrollment | 60 |
Est. completion date | August 11, 2020 |
Est. primary completion date | August 11, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 16 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Patients with American Society of Anesthesiologist (ASA) classification <2 - Patients with chronic with or without nasal polyposis refractory to medical treatment Exclusion Criteria: - Patients with a history of of bleeding diathesis - Patients with severe ischemic heart disease , pulmonary and renal disease - Patients with tumours or vascular anomalies - Patients with cystic fibrosis, allergic fungal sinusitis and granulomatous disorders - Patients who are unable to speak, read and write English |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Jordan University of Science and Technology |
Gan EC, Alsaleh S, Manji J, Habib AR, Amanian A, Javer AR. Hemostatic effect of hot saline irrigation during functional endoscopic sinus surgery: a randomized controlled trial. Int Forum Allergy Rhinol. 2014 Nov;4(11):877-84. doi: 10.1002/alr.21376. Epub — View Citation
Higgins TS, Hwang PH, Kingdom TT, Orlandi RR, Stammberger H, Han JK. Systematic review of topical vasoconstrictors in endoscopic sinus surgery. Laryngoscope. 2011 Feb;121(2):422-32. doi: 10.1002/lary.21286. Epub 2011 Jan 13. Review. — View Citation
Khosla AJ, Pernas FG, Maeso PA. Meta-analysis and literature review of techniques to achieve hemostasis in endoscopic sinus surgery. Int Forum Allergy Rhinol. 2013 Jun;3(6):482-7. doi: 10.1002/alr.21126. Epub 2012 Dec 16. Review. — View Citation
Saif AM, Farboud A, Delfosse E, Pope L, Adke M. Assessing the safety and efficacy of drugs used in preparing the nose for diagnostic and therapeutic procedures: a systematic review. Clin Otolaryngol. 2016 Oct;41(5):546-63. doi: 10.1111/coa.12563. Epub 201 — View Citation
Yim MT, Ahmed OG, Takashima M. Evaluating real-time effects of topical 1:1000 epinephrine in endoscopic sinus and skull-base surgery on hemodynamic parameters through intraoperative arterial line monitoring. Int Forum Allergy Rhinol. 2017 Nov;7(11):1065-1 — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The Boezaart intraoperative surgical field scale | The Boezaart intra-operative surgical field scale will be used to grade the level of bleeding during surgery. This 0 to 5-point scale will be used to outline the amount of suction required to rid the area of blood disrupting vision. A score of 0 is given for an area with no bleeding, 1 for slight bleeding with no suction required, 2 for slight bleeding requiring suction, 3 for moderate bleeding which improves for several seconds once suction has occurred, 4 for moderate bleeding which restarts directly after suctioning and 5 for severe bleeding which occurs faster then can be removed | 2 hours | |
Secondary | Volume of total blood loss | Total blood loss will be calculated and measured over the duration of surgery. | The volume of blood loss will be measured every 30 minutes from the start of surgery for the duration of 2 hours |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05895929 -
The Role of IL5 in Epithelial Cell Integrity
|
Early Phase 1 | |
Completed |
NCT03673956 -
Topical Antibiotics in Chronic Rhinosinusitis
|
Phase 1/Phase 2 | |
Recruiting |
NCT03970655 -
Functional Endoscopic Sinus Surgery Study
|
Phase 1/Phase 2 | |
Not yet recruiting |
NCT04514120 -
Alsaleh-Javer Endoscopic Sinus Score (AJESS) System
|
N/A | |
Recruiting |
NCT03963648 -
NO Measurements in Screening for Asthma and OSA, in Patients With CRSwNP
|
N/A | |
Recruiting |
NCT05009758 -
Moving Towards Precision Medicine in United Airways Disease: Unraveling Inflammatory Patterns in Asthmatic Patients With or Without Nasal Polyps
|
N/A | |
Active, not recruiting |
NCT05553951 -
Adherence in Global Airways
|
N/A | |
Completed |
NCT03563521 -
Identifying Serum Cytokine Profiles of Distinct Inflammatory Phenotypes in Severe Asthma
|
||
Completed |
NCT05035654 -
LYR-220 for Adult Subjects With Chronic Rhinosinusitis (BEACON Study)
|
Phase 2 | |
Withdrawn |
NCT03369574 -
Study of Chronic Rhinosinusitis Symptoms in Asthma Patients Undergoing Treatment With Reslizumab
|
||
Recruiting |
NCT05400616 -
Nasal Microbiota Transfer Therapy in Chronic Rhinosinusitis Without Nasal Polyps (CRSsNP)
|
N/A | |
Recruiting |
NCT04628442 -
Tissue Immune Interaction in Nasal Polyposis
|
||
Completed |
NCT04041609 -
LYR-210 Depot (LYR-210) for Adult Subjects With Chronic Sinusitis (LANTERN Study)
|
Phase 2 | |
Completed |
NCT04048070 -
The Effect of Enhanced Recovery After Surgery in Endoscopic Sinus Surgery
|
N/A | |
Recruiting |
NCT03439865 -
Ivacaftor for Acquired CFTR Dysfunction in Chronic Rhinosinusitis
|
Early Phase 1 | |
Recruiting |
NCT05857228 -
Viral and Epigenetic Influences in CRSwNP
|
||
Completed |
NCT03122795 -
Sinonasal Microbiome Transplant as a Therapy for Chronic Rhinosinusitis Without Nasal Polyps (CRSsNP)
|
N/A | |
Recruiting |
NCT05295459 -
Efficacy and Safety of LYR-210 for the Treatment of Chronic Rhinosinusitis in Adults (ENLIGHTEN 2)
|
Phase 3 | |
Completed |
NCT04858802 -
A Clinical Evaluation of PROPEL® Contour Sinus Implant
|
N/A | |
Completed |
NCT04572516 -
Botulium Toxin Type A In Non Infectious Chronic Rhinosinusitis
|
Phase 3 |