Primary Objective: The goal of this pilot study is to evaluate whether optical spectroscopy is able to differentiate between nerve tissue and surrounding tissue. Secondary Objective: During the measurement procedure, possible improvements of…
ID
Bron
Aandoening
The study is designed as an observational pilot study. The measured diffuse reflectance and fluorescence spectra acquired in this pilot study will not be shared with the physicians during the interventional procedure.
Patients eligible for inclusion into this study are patients admitted to The Netherlands Cancer Institute (NKI-AvL) for elective surgery.
Suitable patients are patients scheduled for:
- inguinal or axillary lymph node dissection (femoral nerve and side braches, thoracodorsal nerve)
- cervical lymph node dissection (great auricular nerve)
- parotidectomy (facial nerve)
- rectal resection for rectal carcinoma
- soft tissue tumour resection
Ondersteuning
HTC34
5656 AE Eindhoven
HTC34
5656 AE Eindhoven
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The ability of optical spectroscopy to differentiate between nerve tissue and surrounding tissue.
Achtergrond van het onderzoek
N/A
Doel van het onderzoek
Primary Objective:
The goal of this pilot study is to evaluate whether optical spectroscopy is able to differentiate between nerve tissue and surrounding tissue.
Secondary Objective:
During the measurement procedure, possible improvements of the measurement hardware will be recorded and the handling during surgery will be evaluated.
Onderzoeksopzet
N/A
Onderzoeksproduct en/of interventie
N/A
Publiek
Plesmanlaan 121
N. Langhout
Amsterdam 1066 CX
The Netherlands
Wetenschappelijk
Plesmanlaan 121
N. Langhout
Amsterdam 1066 CX
The Netherlands
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Patients planned for elective inguinal, axillary or cervical lymph node dissection or parotidectomy , patients with rectal cancer undergoing rectal surgery and patients undergoing resection of a soft tissue tumour;
2. Patients that have provided a signed informed consent;
3. Patients ≥ 18 years old.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Patients with suspected sensitivity to light; e.g. patients who have had photodynamic therapy.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL3577 |
| NTR-old | NTR3735 |
| CCMO | NL40893.031.12 |
| ISRCTN | ISRCTN wordt niet meer aangevraagd. |
| OMON | NL-OMON37194 |