Clinical trials: Body Fluid Leakage
Amniotic Problems
Pivotal Study of the Rx Al-Sense Liner for Amniotic Fluid Leakage Screening
This is a Prospective open-label, comparative pivotal study with comparison of self-assessments with blinded investigator assessments.
- Trial name
- PRALS (NCT02959268)
- Testing
- Al-Sense
- Where
- 4 sites in United States
- Volunteers
- 250 people, healthy volunteers welcome
- Sponsor
- Common Sense
Rupture of Amniotic Membranes
Analysis of ROM Plus to Detect Rupture of Membranes
Specific objectives include confirmation: i) that the ROM PLUS consistently and accurately diagnoses rupture of membranes (ROM), ii) that the technique can be understood and applied in clinical practice, and iii) that the ROM…
- Trial name
- NCT01366443
- Testing
- Sterile speculum exam, ROM Plus Exam, Chart Reveiw
- Where
- United States
- Volunteers
- 288 people, healthy volunteers welcome
- Sponsor
- Clinical Innovations, LLC
AMNIOTIC FLUID LEAKAGE
Pivotal Study of the AL-SENSE in Diagnosis Amniotic Fluid Leakage
This study is designed to demonstrate that the performance of the AL-SENSE developed by Common Sense Ltd. is safe and effective and can be used to indicate if the patient may be experiencing an amniotic fluid leakage or a "water…
- Trial name
- NCT03190434
- Testing
- AL-SENSE
- Volunteers
- 340 people, healthy volunteers welcome
- Sponsor
- Common Sense
Skull Base Neoplasms, Cerebrospinal Fluid Leakage
Role of Novel RADA16 Hydrogel in Endoscopic Skull Base Surgery
The purpose of this study is to specifically evaluate the effectiveness of PuraGel, a RADA16 polypeptide hydrogel, in expediting post-operative healing and re-mucosalization of the nasoseptal flap harvest site during endoscopic…
- Conditions
- Skull Base Neoplasms, Cerebrospinal Fluid Leakage, Nasal; Hypertrophy, Mucous Membrane (Septum)
- Trial name
- NCT05898074
- Testing
- Non-Absorbable Packing (Silastic Splint), PuraGel (RADA16) Hydrogel
- Where
- United States
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Indiana University
Amniotic Fluid Leakage
Study of a Diagnostic Device for Identifying Between Amniotic Fluid to Urine
The purpose of this study is to compare the reliability and validity of a new device with standard methods for diagnosing between amniotic fluid leakage due to premature rupture of the membranes (PROM) and urine.
- Trial name
- NCT01517633
- Testing
- BirthSign
- Where
- Israel
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Hadassah Medical Organization