Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03697642
Other study ID # 201800138A3
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 24, 2018
Est. completion date September 3, 2019

Study information

Verified date April 2019
Source Chang Gung Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Nasogastric tube placement is essential for various surgery and critically ill patients. However, NG tube insertion in anesthetized, paralyzed, and intubated or unconscious patients may be difficult, with reported success rate less 50% on the first attempt without any auxiliary devices. Endotracheal tube intubation narrow the space of oropharynx and hypopharynx. Loss ability to swallow and tongue drop also made the NG tube coil in the mouth easily. Investigators assume nasopharyngeal airway can facilitate NG tube insertion by opening a channel from nostril to epiglottis and reduce complications by protecting nasal cavity while inserting NG.


Recruitment information / eligibility

Status Completed
Enrollment 108
Est. completion date September 3, 2019
Est. primary completion date September 3, 2019
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Patient should be > 20 years old, ASA 1~3 under going schedule general anesthesia with endotracheal tube intubation

- Patient who required NG tube placement for perioperative care

Exclusion Criteria:

- Coagulation abnormality (PLT=100000, INR>1.2 & PT=13)

- Hemodynamic unstable (with inotropic agent use)

- Arrythmia

- Esophageal varices or stricture, Esophageal cancer, trauma or previous esophageal surgery

- Gastric cancer involve cardiac orifice

- Corrosive chemical (strong acid or alkali) ingestion

- Skull base fracture

- Recent nasal surgery, nasal fracture or severe nasal obstruction

- Loose teeth that make endotracheal tube can not fix right side

Study Design


Intervention

Procedure:
With nasopharyngeal airway
Nasopharyngeal airway is previously inserted into selected nostril. NG tube is properly lubricated and placed through Nasopharyngeal airway.
Without nasopharyngeal airway
NG tube is properly lubricated and placed into selected nostril

Locations

Country Name City State
Taiwan Chang Gung Memorial Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
Chang Gung Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary First attempt successful rate with or without Nasopharyngeal airway assistance can be know after NG tube placement immediately
Primary Second attempt successful rate with or without Nasopharyngeal airway assistance can be know after NG tube placement immediately
Primary Overall successful rate insertion with or without Nasopharyngeal airway assistance can be know after NG tube placement immediately
Primary Time cost during NG tube placement with or without Nasopharyngeal airway assistance can be know after NG tube placement immediately
Secondary Incidence of NG tube coiling with or without Nasopharyngeal airway assistance during NG tube insertion can be know after NG tube placement immediately
Secondary Incidence of NG tube kinking with or without Nasopharyngeal airway assistance during NG tube insertion can be know after NG tube placement immediately
Secondary Incidence of NG tube knotting with or without Nasopharyngeal airway assistance during NG tube insertion can be know after NG tube placement immediately
Secondary Incidence of epistaxis after NG tube placement with or without Nasopharyngeal airway assistance during NG tube insertion can be know after NG tube placement immediately
Secondary Mean blood pressure change after NG tube placement with or without Nasopharyngeal airway assistance can be know after NG tube placement immediately
Secondary Heart rate change after NG tube placement with or without Nasopharyngeal airway assistance can be know after NG tube placement immediately
See also
  Status Clinical Trial Phase
Recruiting NCT06063798 - Respiratory Effects of Flow-Controlled Ventilation and Jet Ventilation in Patients Undergoing Laryngotracheal Surgery N/A
Not yet recruiting NCT05035069 - Efficacy and Safety of Ciprofol Compared to Propofol for Nonintubated General Anesthesia in Patients Undergoing TAVR Phase 4
Completed NCT03861364 - Hemodynamics During Induction of General Anesthesia With High and Low Propofol Dose. Phase 4
Completed NCT02711280 - The Effect of Anesthetics on Oxidative Stress and Apoptosis Status in Children N/A
Completed NCT01199471 - Estimate the Behavior of Chinese Anesthesiologists Practicing General Anesthesia With Sevoflurane N/A
Completed NCT00917033 - Tracheal Intubation of Morbidly Obese Patients. GlideScope Versus Direct Laryngoscopy Phase 4
Completed NCT00391885 - Target-controlled Infusion of Propofol and Remifentanil During General Anaesthesia Guided by Entropy Phase 4
Completed NCT00552617 - A Bridging Trial Comparing Sugammadex (Org 25969) at Reappearance of T2 in Japanese and Caucasian Participants. Part B: Caucasian Participants (P05971) Phase 2
Completed NCT03705026 - Relationship Between Genetic Polymorphism and Postoperative Nausea and Vomiting in Chinese Han Population
Completed NCT00552929 - A Bridging Trial Comparing Sugammadex (Org 25969) at 1-2 Post-Tetanic Count (PTC) in Caucasian Participants. Part B (P05974) Phase 2
Completed NCT00475215 - Safety and Efficacy of Sugammadex (Org 25969, MK-8616) in Participants With or Having a Past History of Pulmonary Disease (19.4.308) (P05932) (MK-8616-017) Phase 3
Completed NCT00298831 - Use of Sugammadex at the End of Case in Routine Anesthesia (MK-8616-023) Phase 3
Recruiting NCT03943745 - EEG Changes During Induction of Propofol Anesthesia
Completed NCT04595591 - Observation of Propofol Titration at Different Speeds N/A
Not yet recruiting NCT05841316 - The ED95 Dose of Sugammadex to Reverse Rocuronium-Induced Deep Neuromuscular Block Back to Shallow Neuromuscular Block
Completed NCT04532502 - Impact of Anesthetic Environment the Sex Ratio of the Children of Female Assistants
Completed NCT03330236 - EEG - Guided Anesthetic Care and Postoperative Delirium N/A
Recruiting NCT06205212 - High-flow Nasal Oxygenation During Preoxygenation and Atelectasis N/A
Completed NCT00379613 - Use of Sugammadex Administered at 5 Minutes After Administration of 1.2 mg/kg Esmeron® (19.4.205)(P05942) Phase 2
Completed NCT03841890 - The Clarus Video System and Direct Laryngoscope for Rapid Sequence Induction Intubation With Cricoid Pressure N/A