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The Effect of desmopressin administration on intraoperative blood loss of sinus surgery

The Effect of nasal spray of desmopressin administration on intraoperative blood loss and quality of the surgical field during functional endoscopic sinus surgery in patients with chronic rhino sinusitis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20101026005026N9
Enrollment
60
Registered
2018-05-08
Start date
2017-12-22
Completion date
Unknown
Last updated
2018-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bleeding during endoscopic surgery of sinuses (FESS). Chronic sinusitis

Interventions

Intervention 1: One puff Desmopressin nasal spray (10 µg) in either nostril before anesthesia. Intervention 2: One puff nasal spray of normal saline in either nostril before anesthesia.

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: All patients must be 18–65 years old, who it is their first-time candidates for two-side FESS

Exclusion criteria

Exclusion criteria: Patients with a history of bleeding disorders or taking medications that may affect surgical homeostasis; Poorly controlled hypertension or cerebrovascular disease; A history of significant coronary artery disease or arrhythmia Secondary surgery Pregnancy A compromised renal or hepatic function; and

Design outcomes

Primary

MeasureTime frame
Intraoperative blood loss. Timepoint: Every 15 minuets from the begining of anesthesia until maximum 90 minutes. Method of measurement: Final intraoperative blood loss was confirmed at the end of each procedure by accounting for loss of blood and irrigation fluid into the suction canister, and nasopharyngeal packing (measured weight of packing on the electronic scale).;Quality of the surgical field during functional endoscopic sinus surgery. Timepoint: End of surgery. Method of measurement: A scoring scale adapted from Boezaart and van der merew.

Secondary

MeasureTime frame
Bleeding after the surgery. Timepoint: Until 4 days after surgery. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasood Mohseni

Iran University of Medical Sciences

masood.mohseni@gmail.com+98 21 6435 2326

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026