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The Effect of Pharyngeal Packing on Postoperative Gastric Volume in Patients Undergoing Nasal Surgery

Investigation of the Effect of Pharyngeal Packing on Postoperative Gastric Volume in Patients Undergoing Nasal Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04819659
Enrollment
180
Registered
2021-03-29
Start date
2021-01-01
Completion date
2022-04-14
Last updated
2022-04-15

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

Conditions

Anesthesia, Gastric Volume, Nasal Surgery, Pharyngeal Packing, Postoperative Nausea

Brief summary

Pharyngeal packing is a frequently used application to reduce the incidence and severity of postoperative nausea and vomiting (PONV) in patients who undergo nasal surgery. This study aims to research the effects of PP on gastric antral cross-sectional area (ACSA) and hence gastric volume as assessed by ultrasound, therewithal PONV and sore throat were evaluated as secondary outcomes in rhino logic surgeries (Septorhinoplasty, Septoplasty, Functional endoscopic sinus surgery).

Detailed description

Postoperative nausea and vomiting (PONV) after nasal surgery (Septorhinoplasty, Septoplasty, Functional endoscopic sinus surgery) is a very common complication (34-60%). Therefore, pharangeal packing was performed to prevent blood ingestion so as to decrease the incidence of PONV and the risk of aspiration. Also, gastric blood is known to be a powerful emetic. Actually, there is not any evidence in the literature reporting the quantitative values of gastric volumes due to blood ingestion. The aim of this study is to research the effect of pharyngeal packing on the perioperative gastric antral cross-sectional area (ACSA) so the gastric volumes. Measurements were performed by ultrasound with convex probe in right lateral decubitus position, in order to evaluate the effectiveness of pharyngeal packing in patients undergoing nasal surgery, and to show its effects on PONV and sore throat.

Interventions

DEVICEPharyngeal packing

Placing gauze-like material in the nasal cavity to absorb blood or other fluids right after tracheal intubation.

Sponsors

Istanbul University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* undergoing elective nasal or paranasal sinus surgery following overnight fasting * 18-70 years of age * accepting to join the study * American Society of Anesthesiologist (ASA) classification system I-III * Body mass Index (BMI) \< 30 kg/m2

Exclusion criteria

* ASA classification higher than III * Age younger than 18 years * BMI\>30 kg/m2 * Preoperative vomiting or antiemetic medication therapy * Intubation needing more than two laryngoscopy attempts * Not agreeing to participate in the study * Coagulation disorders * Diseases or conditions affecting gastric volume or motility

Design outcomes

Primary

MeasureTime frameDescription
The crosssectional area (ACSA) (Postoperative) (mm2) (Postoperative)10 minutes before extubationmeasurements are done with USG and calculated with this formula CSA = (AP (anterior-posterior) diameter × CC (cranio-caudal) diameter× 3.14) / 4.

Secondary

MeasureTime frameDescription
Postoperative presence and severity of PONVat the first, second and 24th hours in PACU and at the wardThe severity of PONV was assessed according to the four points score: None (0 point), nausea (1 point), nausea with maximum of two vomiting episodes (2 points), more than two vomiting episodes (3 points). When PONV with ≥ 2 points metaclopropamid 10 mg was done, and in order to repetition granisetron 3 mg was added.
The severity of sore throatat the first, second and 24th hours in PACU and at the wardNo pain (0 point), mild pain (1 point), moderate pain (2 points) and severe pain (3 points). Patients with severe sore throat were given paracetamol.
Blood volume in the suction systemin the perioperative periodweighing sponge, pad, compress and blood volume in the aspirator

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026